A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043703



Internal ID18786234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83931002..83988630hg38UCSC Ensembl
Innerchr9:86545917..86603545hg19UCSC Ensembl
Innerchr9:85735737..85793365hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3857629
hg1957629
hg1857629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697524
Samples
Known GenesC9orf64, HNRNPK, MIR7-1, RMI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043703
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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