A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528105



Internal ID15455398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45858902..45872867hg38UCSC Ensembl
Innerchr6:45826639..45840604hg19UCSC Ensembl
Innerchr6:45934617..45948582hg18UCSC Ensembl
Innerchr6:45934617..45948582hg17UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3813966
hg1913966
hg1813966
hg1713966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704646
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528105
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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