A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524329



Internal ID15451622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212458051..212461241hg38UCSC Ensembl
Innerchr1:212631393..212634583hg19UCSC Ensembl
Innerchr1:210698016..210701206hg18UCSC Ensembl
Innerchr1:209019788..209022978hg17UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg383191
hg193191
hg183191
hg173191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700235
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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