A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3479921



Internal ID18722213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16684943..16934704hg38UCSC Ensembl
Innerchr1:17011438..17261199hg19UCSC Ensembl
Innerchr1:16884025..17133786hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38249762
hg19249762
hg18249762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999163
Supporting Variants
Samples
Known GenesCROCC, ESPNP, LOC729574, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3479921
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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