A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598441



Internal ID16039164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69538215..69605029hg38UCSC Ensembl
Innerchr5:68834042..68900856hg19UCSC Ensembl
Innerchr5:68869798..68936612hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3866815
hg1966815
hg1866815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9834n54
Supporting Variantsnssv1034677
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)nsv598441
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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