A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002599



Internal ID18745131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16912960..16968705hg38UCSC Ensembl
Innerchr1:17239455..17295200hg19UCSC Ensembl
Innerchr1:17112042..17167787hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3855746
hg1955746
hg1855746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3481639
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002599
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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