A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525193



Internal ID15105800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75565133..75576296hg38UCSC Ensembl
Innerchr11:75276178..75287341hg19UCSC Ensembl
Innerchr11:74953826..74964989hg18UCSC Ensembl
Innerchr11:74953826..74964989hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3811164
hg1911164
hg1811164
hg1711164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701272
Samples
Known GenesSERPINH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525193
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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