A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528903



Internal ID15456196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:78540526..78566708hg38UCSC Ensembl
Innerchr13:79114661..79140843hg19UCSC Ensembl
Innerchr13:78012662..78038844hg18UCSC Ensembl
Innerchr13:78012662..78038844hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3826183
hg1926183
hg1826183
hg1726183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv114n21
Supporting Variantsnssv705587
Samples
Known GenesRNF219-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528903
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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