A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3470452



Internal ID18717249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16643019hg38UCSC Ensembl
Innerchr1:16871266..16969514hg19UCSC Ensembl
Innerchr1:16743853..16842101hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3898249
hg1998249
hg1898249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006436
Supporting Variants
Samples
Known GenesCROCCP2, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3470452
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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