A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026445



Internal ID19115663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64965592hg38UCSC Ensembl
Innerchr9:69474914..69978010hg19UCSC Ensembl
Innerchr9:68764734..69267830hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38503097
hg19503097
hg18503097
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7658n100
Supporting Variantsnssv3696136, nssv3696137
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)nsv1026445
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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