A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611732



Internal ID6998637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170255438..170258870hg38UCSC Ensembl
Innerchr6:170255438..170258870hg38UCSC Ensembl
Outerchr6:170255223..170259101hg38UCSC Ensembl
chr6:170564526..170567958hg19UCSC Ensembl
Innerchr6:170564526..170567958hg19UCSC Ensembl
Outerchr6:170564311..170568189hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383433
hg193433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12653376, essv12653374, essv12653372, essv12653373, essv12653375, essv12653377, essv12653378
SamplesHG03484, HG02702, HG02852, HG01366, HG03079, HG00182, HG02594
Known GenesLOC154449
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611732
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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