A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522265



Internal ID15449558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15493946..15545982hg38UCSC Ensembl
Innerchr6:15494177..15546213hg19UCSC Ensembl
Innerchr6:15602156..15654192hg18UCSC Ensembl
Innerchr6:15602156..15654192hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3852037
hg1952037
hg1852037
hg1752037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695045
Samples
Known GenesDTNBP1, JARID2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522265
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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