A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525078



Internal ID15452371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97095914..97174000hg38UCSC Ensembl
Innerchr11:96966914..97045000hg19UCSC Ensembl
Innerchr11:96472124..96550210hg18UCSC Ensembl
Innerchr11:96472124..96550210hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3878087
hg1978087
hg1878087
hg1778087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701133
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525078
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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