A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997887



Internal ID18810737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15994515..16115208hg38UCSC Ensembl
Innerchr1:16321010..16441703hg19UCSC Ensembl
Innerchr1:16193597..16314290hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38120694
hg19120694
hg18120694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3698789
Samples
Known GenesC1orf64, CLCNKA, CLCNKB, FAM131C, HSPB7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997887
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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