A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516628



Internal ID15443921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73961328..74010800hg38UCSC Ensembl
Innerchr9:76576244..76625716hg19UCSC Ensembl
Innerchr9:75766064..75815536hg18UCSC Ensembl
Innerchr9:73805798..73855270hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3849473
hg1949473
hg1849473
hg1749473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669699, nssv654744
Samples
Known GenesMIR6130
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516628
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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