A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526525



Internal ID15107132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76992319..76993271hg38UCSC Ensembl
Innerchr18:74704275..74705227hg19UCSC Ensembl
Innerchr18:72833263..72834215hg18UCSC Ensembl
Innerchr18:72833263..72834215hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38953
hg19953
hg18953
hg17953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702837
Samples
Known GenesMBP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526525
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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