A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12174505



Internal ID2642893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1661035..1661492hg38UCSC Ensembl
Innerchr6:1661085..1661442hg38UCSC Ensembl
Outerchr6:1660985..1661542hg38UCSC Ensembl
chr6:1661269..1661726hg19UCSC Ensembl
Innerchr6:1661319..1661676hg19UCSC Ensembl
Outerchr6:1661219..1661776hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607894
Supporting Variants
SamplesHG02337
Known GenesGMDS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12174505
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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