A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12599694



Internal ID6303955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155784367..155807154hg38UCSC Ensembl
Innerchr6:155784369..155807153hg38UCSC Ensembl
Outerchr6:155784366..155807156hg38UCSC Ensembl
chr6:156105501..156128288hg19UCSC Ensembl
Innerchr6:156105503..156128287hg19UCSC Ensembl
Outerchr6:156105500..156128290hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3822788
hg1922788
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611352
Supporting Variants
SamplesNA19908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12599694
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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