A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3477568



Internal ID18720935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16502007..16876990hg38UCSC Ensembl
Innerchr1:16828502..17203485hg19UCSC Ensembl
Innerchr1:16701089..17076072hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38374984
hg19374984
hg18374984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014379
Supporting Variants
Samples
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, 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)nssv3477568
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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