A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034994



Internal ID15541494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:71009869..71098321hg38UCSC Ensembl
Innerchr5:70305696..70394148hg19UCSC Ensembl
Innerchr5:70341452..70429904hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3888453
hg1988453
hg1888453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598592
Supporting Variants
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)nssv1034994
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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