A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3479025



Internal ID18721736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16617106..16679471hg38UCSC Ensembl
Innerchr1:16943601..17005966hg19UCSC Ensembl
Innerchr1:16816188..16878553hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3862366
hg1962366
hg1862366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998431
Supporting Variants
Samples
Known GenesCROCCP2, LOC729574, MST1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3479025
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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