A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516636



Internal ID15097243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62574020..62584861hg38UCSC Ensembl
Innerchr17:60651381..60662222hg19UCSC Ensembl
Innerchr17:58005113..58015954hg18UCSC Ensembl
Innerchr17:58005113..58015954hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3810842
hg1910842
hg1810842
hg1710842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669771, nssv662833, nssv660104
Samples
Known GenesTLK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516636
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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