A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3475701



Internal ID18719953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16931436hg38UCSC Ensembl
Innerchr1:17203485..17257931hg19UCSC Ensembl
Innerchr1:17076072..17130518hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3854447
hg1954447
hg1854447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999431
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)nssv3475701
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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