A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522573



Internal ID15103180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32828908..32830506hg38UCSC Ensembl
Innerchr6:32796685..32798283hg19UCSC Ensembl
Innerchr6:32904663..32906261hg18UCSC Ensembl
Innerchr6:32904663..32906261hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
hg171599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705957
Samples
Known GenesTAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522573
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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