A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668022



Internal ID15404674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97713776..97760338hg38UCSC Ensembl
Innerchr5:97049480..97096042hg19UCSC Ensembl
Innerchr5:97075236..97121798hg18UCSC Ensembl
Innerchr5:97075236..97121798hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3846563
hg1946563
hg1846563
hg1746563
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)nssv668022
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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