A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523611



Internal ID15104218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74755524..74767659hg38UCSC Ensembl
Innerchr17:72751663..72763798hg19UCSC Ensembl
Innerchr17:70263258..70275393hg18UCSC Ensembl
Innerchr17:70263258..70275393hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3812136
hg1912136
hg1812136
hg1712136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699405
Samples
Known GenesSLC9A3R1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523611
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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