A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009214



Internal ID18751745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16685807hg38UCSC Ensembl
Innerchr1:16871266..17012302hg19UCSC Ensembl
Innerchr1:16743853..16884889hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38141037
hg19141037
hg18141037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n100
Supporting Variantsnssv3482680
Samples
Known GenesCROCCP2, LOC729574, 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)nsv1009214
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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