A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032179



Internal ID19121401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64917802hg38UCSC Ensembl
Innerchr9:69474914..69930220hg19UCSC Ensembl
Innerchr9:68764734..69220040hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38455307
hg19455307
hg18455307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7657n100
Supporting Variantsnssv3696135, nssv3696134
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)nsv1032179
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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