A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034652



Internal ID15541152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69531242..69608851hg38UCSC Ensembl
Innerchr5:68827069..68904678hg19UCSC Ensembl
Innerchr5:68862825..68940434hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3877610
hg1977610
hg1877610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598425
Supporting Variants
Samples
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, LOC647859, OCLN, SMA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1034652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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