A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12608412



Internal ID2610228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159064533..159066667hg38UCSC Ensembl
Innerchr6:159064546..159066655hg38UCSC Ensembl
Outerchr6:159064521..159066680hg38UCSC Ensembl
chr6:159485565..159487699hg19UCSC Ensembl
Innerchr6:159485578..159487687hg19UCSC Ensembl
Outerchr6:159485553..159487712hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382135
hg192135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611411
Supporting Variants
SamplesNA19024
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12608412
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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