A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001952



Internal ID18744483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16525007..16618834hg38UCSC Ensembl
Innerchr1:16851502..16945329hg19UCSC Ensembl
Innerchr1:16724089..16817916hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3893828
hg1993828
hg1893828
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3471132, nssv3698800
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)nsv1001952
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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