A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1038096



Internal ID15891282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94452874..94477180hg38UCSC Ensembl
Innerchr5:93788579..93812885hg19UCSC Ensembl
Innerchr5:93814335..93838641hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3824307
hg1924307
hg1824307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598951
Supporting Variants
Samples
Known GenesKIAA0825
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1038096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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