A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527592



Internal ID15108199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29577938..29582841hg38UCSC Ensembl
Innerchr6:29545715..29550618hg19UCSC Ensembl
Innerchr6:29653694..29658597hg18UCSC Ensembl
Innerchr6:29653694..29658597hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384904
hg194904
hg184904
hg174904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv376n21
Supporting Variantsnssv704053
Samples
Known GenesSNORD32B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527592
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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