A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008952



Internal ID18751483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16525007..16660344hg38UCSC Ensembl
Innerchr1:16851502..16986839hg19UCSC Ensembl
Innerchr1:16724089..16859426hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38135338
hg19135338
hg18135338
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv44n100
Supporting Variantsnssv3698803, nssv3464432, nssv3465324
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)nsv1008952
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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