A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022085



Internal ID19111303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64493516..64820291hg38UCSC Ensembl
Innerchr9:69505934..69832709hg19UCSC Ensembl
Innerchr9:68795754..69122529hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38326776
hg19326776
hg18326776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7655n100
Supporting Variantsnssv3696141
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022085
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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