A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598568



Internal ID16039291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:70969293..71080664hg38UCSC Ensembl
Innerchr5:70265120..70376491hg19UCSC Ensembl
Innerchr5:70300876..70412247hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38111372
hg19111372
hg18111372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9861n54
Supporting Variantsnssv1034951
Samples
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, LOC647859, NAIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598568
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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