A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042177



Internal ID18784708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127263008..127317406hg38UCSC Ensembl
Innerchr9:130025287..130079685hg19UCSC Ensembl
Innerchr9:129065108..129119506hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3854399
hg1954399
hg1854399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695249
Samples
Known GenesGARNL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042177
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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