A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527895



Internal ID15108502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52506621..52516387hg38UCSC Ensembl
Innerchr6:52371419..52381185hg19UCSC Ensembl
Innerchr6:52479378..52489144hg18UCSC Ensembl
Innerchr6:52479378..52489144hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg389767
hg199767
hg189767
hg179767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704398
Samples
Known GenesTRAM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527895
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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