A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517284



Internal ID15097891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152883607..152965776hg38UCSC Ensembl
InnerchrX:152052151..152134320hg19UCSC Ensembl
InnerchrX:151802807..151884976hg18UCSC Ensembl
InnerchrX:151722719..151804888hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3882170
hg1982170
hg1882170
hg1782170
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659888, nssv690116, nssv702281, nssv666686, nssv669107, nssv654201, nssv681042, nssv702600, nssv693822, nssv702025, nssv702101
Samples
Known GenesZNF185
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517284
Frequency
Sample Size2026
Observed Gain9
Observed Loss2
Observed Complex0
Frequencyn/a


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