A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466751



Internal ID18715249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16505368..16660344hg38UCSC Ensembl
Innerchr1:16831863..16986839hg19UCSC Ensembl
Innerchr1:16704450..16859426hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38154977
hg19154977
hg18154977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006224
Supporting Variants
Samples
Known GenesCROCCP2, 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)nssv3466751
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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