A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759838



Internal ID19058119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130745540..130761602hg38UCSC Ensembl
Innerchr9:133620927..133636989hg19UCSC Ensembl
Innerchr9:132610748..132626810hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3816063
hg1916063
hg1816063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049425
Supporting Variants
Samples
Known GenesABL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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