A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517637



Internal ID15444930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102589070..102596713hg38UCSC Ensembl
Innerchr5:101924774..101932417hg19UCSC Ensembl
Innerchr5:101952673..101960316hg18UCSC Ensembl
Innerchr5:101952673..101960316hg17UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg387644
hg197644
hg187644
hg177644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656523, nssv679811, nssv662365, nssv652636, nssv655219, nssv667981, nssv668429, nssv666402, nssv684765, nssv673539, nssv655760, nssv682357, nssv692523, nssv680116, nssv659856, nssv671078, nssv677100, nssv677248
Samples
Known GenesLINC00492
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517637
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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