A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525703



Internal ID15452996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147438398..147446099hg38UCSC Ensembl
Innerchr6:147759534..147767235hg19UCSC Ensembl
Innerchr6:147801227..147808928hg18UCSC Ensembl
Innerchr6:147801227..147808928hg17UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg387702
hg197702
hg187702
hg177702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701863
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525703
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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