A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050510



Internal ID18793041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99922036..99986376hg38UCSC Ensembl
Innerchr9:102684318..102748658hg19UCSC Ensembl
Innerchr9:101724139..101788479hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3864341
hg1964341
hg1864341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697574
Samples
Known GenesERP44, STX17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050510
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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