A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700672



Internal ID15090638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167324194..167326875hg38UCSC Ensembl
Innerchr6:167737682..167740363hg19UCSC Ensembl
Innerchr6:167657672..167660353hg18UCSC Ensembl
Innerchr6:167708093..167710774hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382682
hg192682
hg182682
hg172682
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517210
Supporting Variants
Samples
Known GenesTTLL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700672
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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