A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524844



Internal ID15452137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:60204304..60211776hg38UCSC Ensembl
Innerchr1:60669976..60677448hg19UCSC Ensembl
Innerchr1:60442564..60450036hg18UCSC Ensembl
Innerchr1:60381997..60389469hg17UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg387473
hg197473
hg187473
hg177473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700846
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524844
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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