A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597301



Internal ID16384710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16179085..16180058hg38UCSC Ensembl
Innerchr5:16179194..16180167hg19UCSC Ensembl
Innerchr5:16232194..16233167hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9620n54
Supporting Variantsnssv1026280, nssv1026281
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597301
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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