A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525982



Internal ID15453275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55445714..55454175hg38UCSC Ensembl
Innerchr8:56358274..56366735hg19UCSC Ensembl
Innerchr8:56520828..56529289hg18UCSC Ensembl
Innerchr8:56520828..56529289hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg388462
hg198462
hg188462
hg178462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702201
Samples
Known GenesSBF1P1, XKR4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525982
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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