A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032134



Internal ID19121356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..254609hg38UCSC Ensembl
Innerchr9:162695..254609hg19UCSC Ensembl
Innerchr9:152695..244609hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3891915
hg1991915
hg1891915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690965
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)nsv1032134
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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