A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611266



Internal ID6998176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151433077..151437058hg38UCSC Ensembl
Innerchr6:151433077..151437058hg38UCSC Ensembl
Outerchr6:151432996..151437227hg38UCSC Ensembl
chr6:151754212..151758193hg19UCSC Ensembl
Innerchr6:151754212..151758193hg19UCSC Ensembl
Outerchr6:151754131..151758362hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383982
hg193982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12584014, essv12584013
SamplesNA19914, HG02439
Known GenesRMND1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611266
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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