A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519934



Internal ID15100541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49841502..49886614hg38UCSC Ensembl
Innerchr10:51049548..51094660hg19UCSC Ensembl
Innerchr10:50719554..50764666hg18UCSC Ensembl
Innerchr10:50719554..50764666hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3845113
hg1945113
hg1845113
hg1745113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674490, nssv677257, nssv660287, nssv659553
Samples
Known GenesPARG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519934
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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