A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597611



Internal ID16385020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25494896..26112083hg38UCSC Ensembl
Innerchr5:25495005..26112192hg19UCSC Ensembl
Innerchr5:25530762..26147949hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38617188
hg19617188
hg18617188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1027974
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597611
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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