A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024881



Internal ID19114098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64903011hg38UCSC Ensembl
Innerchr9:69474914..69915429hg19UCSC Ensembl
Innerchr9:68764734..69205249hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38440516
hg19440516
hg18440516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7657n100
Supporting Variantsnssv3696132, nssv3696133
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)nsv1024881
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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