A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524951



Internal ID15105558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36102943..36153146hg38UCSC Ensembl
Innerchr17:34430336..34480526hg19UCSC Ensembl
Innerchr17:31454449..31504639hg18UCSC Ensembl
Innerchr17:31454449..31504639hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3850204
hg1950191
hg1850191
hg1750191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv178n21
Supporting Variantsnssv700971
Samples
Known GenesCCL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524951
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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