A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668429



Internal ID15405081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102589070..102594984hg38UCSC Ensembl
Innerchr5:101924774..101930688hg19UCSC Ensembl
Innerchr5:101952673..101958587hg18UCSC Ensembl
Innerchr5:101952673..101958587hg17UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg385915
hg195915
hg185915
hg175915
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517637
Supporting Variants
Samples
Known GenesLINC00492
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668429
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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