A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516844



Internal ID15097451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102955808..103236914hg38UCSC Ensembl
Innerchr9:105718090..105999196hg19UCSC Ensembl
Innerchr9:104757911..105039017hg18UCSC Ensembl
Innerchr9:102797645..103078751hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38281107
hg19281107
hg18281107
hg17281107
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695601, nssv706068, nssv694078, nssv682089, nssv654396, nssv699852, nssv695702
Samples
Known GenesCYLC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516844
Frequency
Sample Size2026
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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