A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3482680



Internal ID18723666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16685807hg38UCSC Ensembl
Innerchr1:16871266..17012302hg19UCSC Ensembl
Innerchr1:16743853..16884889hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38141037
hg19141037
hg18141037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009214
Supporting Variants
Samples
Known GenesCROCCP2, LOC729574, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3482680
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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