A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645945



Internal ID7032691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46096958..46097392hg38UCSC Ensembl
Innerchr20:46096963..46097388hg38UCSC Ensembl
Outerchr20:46096954..46097397hg38UCSC Ensembl
chr20:44725597..44726031hg19UCSC Ensembl
Innerchr20:44725602..44726027hg19UCSC Ensembl
Outerchr20:44725593..44726036hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16196692, essv16196686, essv16196678, essv16196684, essv16196679, essv16196688, essv16196687, essv16196677, essv16196693, essv16196673, essv16196674, essv16196694, essv16196691, essv16196683, essv16196680, essv16196675, essv16196681, essv16196682, essv16196676, essv16196689, essv16196685, essv16196690
SamplesNA19141, HG03100, NA18504, NA19098, NA19171, HG01350, HG03091, NA18923, HG02281, NA19200, HG03054, HG01882, HG03457, HG02953, HG03458, NA18865, NA19143, HG01556, NA19093, HG01883, NA19121, HG02947
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645945
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer