A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12179396



Internal ID3620238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3918076..3927339hg38UCSC Ensembl
Innerchr6:3918576..3926839hg38UCSC Ensembl
Outerchr6:3917076..3928339hg38UCSC Ensembl
chr6:3918310..3927573hg19UCSC Ensembl
Innerchr6:3918810..3927073hg19UCSC Ensembl
Outerchr6:3917310..3928573hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg389264
hg199264
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607937
Supporting Variants
SamplesHG03212
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12179396
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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