A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607894



Internal ID6994825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1661035..1661492hg38UCSC Ensembl
Innerchr6:1661085..1661442hg38UCSC Ensembl
Outerchr6:1660985..1661542hg38UCSC Ensembl
chr6:1661269..1661726hg19UCSC Ensembl
Innerchr6:1661319..1661676hg19UCSC Ensembl
Outerchr6:1661219..1661776hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12174505
SamplesHG02337
Known GenesGMDS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607894
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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