A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519538



Internal ID15100145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:44002563..44003359hg38UCSC Ensembl
Innerchr1:44468235..44469031hg19UCSC Ensembl
Innerchr1:44240822..44241618hg18UCSC Ensembl
Innerchr1:44137328..44138124hg17UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38797
hg19797
hg18797
hg17797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681965, nssv656769, nssv661267
Samples
Known GenesSLC6A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519538
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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