A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699363



Internal ID15089329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59527314..59605717hg38UCSC Ensembl
Innerchr1:59992986..60071389hg19UCSC Ensembl
Innerchr1:59765574..59843977hg18UCSC Ensembl
Innerchr1:59705007..59783410hg17UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3878404
hg1978404
hg1878404
hg1778404
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523577
Supporting Variants
Samples
Known GenesFGGY
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699363
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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