A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026697



Internal ID19115915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64500903..64965592hg38UCSC Ensembl
Innerchr9:69513321..69978010hg19UCSC Ensembl
Innerchr9:68803141..69267830hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38464690
hg19464690
hg18464690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7659n100
Supporting Variantsnssv3696150
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)nsv1026697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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