A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687249



Internal ID15423901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97713776..97801352hg38UCSC Ensembl
Innerchr5:97049480..97137056hg19UCSC Ensembl
Innerchr5:97075236..97162812hg18UCSC Ensembl
Innerchr5:97075236..97162812hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3887577
hg1987577
hg1887577
hg1787577
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)nssv687249
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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