A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704121



Internal ID15440773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97448022..97924654hg38UCSC Ensembl
Innerchr5:96783726..97260358hg19UCSC Ensembl
Innerchr5:96809482..97286114hg18UCSC Ensembl
Innerchr5:96809482..97286114hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38476633
hg19476633
hg18476633
hg17476633
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527650
Supporting Variants
Samples
Known GenesLOC102546227
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704121
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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