A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516794



Internal ID15097401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128082600..128109361hg38UCSC Ensembl
Innerchr6:128403745..128430506hg19UCSC Ensembl
Innerchr6:128445438..128472199hg18UCSC Ensembl
Innerchr6:128445438..128472199hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3826762
hg1926762
hg1826762
hg1726762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693267, nssv670919
Samples
Known GenesPTPRK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516794
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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