A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695209



Internal ID15431861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40723631..40725664hg38UCSC Ensembl
Innerchr6:40691370..40693403hg19UCSC Ensembl
Innerchr6:40799348..40801381hg18UCSC Ensembl
Innerchr6:40799348..40801381hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382034
hg192034
hg182034
hg172034
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517805
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695209
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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