A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014816



Internal ID18757351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:19427353..19449317hg38UCSC Ensembl
Innerchr1:19753847..19775811hg19UCSC Ensembl
Innerchr1:19626434..19648398hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821965
hg1921965
hg1821965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3478468
Samples
Known GenesCAPZB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014816
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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