A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051764



Internal ID18794295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69074840..69101139hg38UCSC Ensembl
Innerchr9:71689756..71716055hg19UCSC Ensembl
Innerchr9:70879576..70905875hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3826300
hg1926300
hg1826300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7667n100
Supporting Variantsnssv3696225
Samples
Known GenesFXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051764
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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