A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031437



Internal ID19120659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..272950hg38UCSC Ensembl
Innerchr9:162695..272950hg19UCSC Ensembl
Innerchr9:152695..262950hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38110256
hg19110256
hg18110256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7349n100
Supporting Variantsnssv3690968, nssv3690969, nssv3758059, nssv3690970
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031437
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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