A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013756



Internal ID18756288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16641704hg38UCSC Ensembl
Innerchr1:16871266..16968199hg19UCSC Ensembl
Innerchr1:16743853..16840786hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3896934
hg1996934
hg1896934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv46n100
Supporting Variantsnssv3476963
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)nsv1013756
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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