A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469806



Internal ID18716892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16919676hg38UCSC Ensembl
Innerchr1:17203485..17246171hg19UCSC Ensembl
Innerchr1:17076072..17118758hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842687
hg1942687
hg1842687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004370
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3469806
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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