A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690693



Internal ID15427345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:96746568..96761378hg38UCSC Ensembl
Innerchr6:97194444..97209254hg19UCSC Ensembl
Innerchr6:97301165..97315975hg18UCSC Ensembl
Innerchr6:97301165..97315975hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3814811
hg1914811
hg1814811
hg1714811
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516517
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690693
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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