A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690649



Internal ID15427301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97712762..97772922hg38UCSC Ensembl
Innerchr5:97048466..97108626hg19UCSC Ensembl
Innerchr5:97074222..97134382hg18UCSC Ensembl
Innerchr5:97074222..97134382hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3860161
hg1960161
hg1860161
hg1760161
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517188
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690649
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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