A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041191



Internal ID19130410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86163605..86275836hg38UCSC Ensembl
Innerchr9:88778520..88890751hg19UCSC Ensembl
Innerchr9:87968340..88080571hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38112232
hg19112232
hg18112232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697536
Samples
Known GenesC9orf153, ISCA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041191
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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