A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520482



Internal ID15101089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203799200..203831298hg38UCSC Ensembl
Innerchr1:203768328..203800426hg19UCSC Ensembl
Innerchr1:202034951..202067049hg18UCSC Ensembl
Innerchr1:200499985..200532083hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3832099
hg1932099
hg1832099
hg1732099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671804, nssv676246, nssv677636, nssv679660, nssv692396
Samples
Known GenesZBED6, ZC3H11A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520482
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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