A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3471540



Internal ID18717819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16931994hg38UCSC Ensembl
Innerchr1:17203485..17258489hg19UCSC Ensembl
Innerchr1:17076072..17131076hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3855005
hg1955005
hg1855005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002908
Supporting Variants
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3471540
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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