A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048135



Internal ID18790666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97904649..97954748hg38UCSC Ensembl
Innerchr9:100666931..100717030hg19UCSC Ensembl
Innerchr9:99706752..99756851hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3850100
hg1950100
hg1850100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697572
Samples
Known GenesC9orf156, HEMGN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048135
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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