A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598613



Internal ID16039336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:71011195..71042023hg38UCSC Ensembl
Innerchr5:70307022..70337850hg19UCSC Ensembl
Innerchr5:70342778..70373606hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3830829
hg1930829
hg1830829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9870n54
Supporting Variantsnssv1035042
Samples
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, NAIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598613
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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