A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527495



Internal ID15454788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5008070..5417881hg38UCSC Ensembl
Innerchr9:5008070..5417881hg19UCSC Ensembl
Innerchr9:4998070..5407881hg18UCSC Ensembl
Innerchr9:4998070..5407881hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38409812
hg19409812
hg18409812
hg17409812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703943
Samples
Known GenesINSL4, INSL6, JAK2, PLGRKT, RLN1, RLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527495
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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