A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025280



Internal ID16319236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10760904..10761395hg38UCSC Ensembl
Innerchr5:10761016..10761507hg19UCSC Ensembl
Innerchr5:10814016..10814507hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38492
hg19492
hg18492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597140
Supporting Variants
Samples
Known GenesDAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1025280
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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