A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526236



Internal ID15453529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73853834..73953184hg38UCSC Ensembl
Innerchr6:74563545..74662900hg19UCSC Ensembl
Innerchr6:74620278..74719628hg18UCSC Ensembl
Innerchr6:74620278..74719628hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3899351
hg1999356
hg1899351
hg1799351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702503
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526236
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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