A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525690



Internal ID15452983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155214568..155219096hg38UCSC Ensembl
Innerchr6:155535702..155540230hg19UCSC Ensembl
Innerchr6:155577394..155581922hg18UCSC Ensembl
Innerchr6:155627815..155632343hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg384529
hg194529
hg184529
hg174529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701849
Samples
Known GenesTIAM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525690
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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