A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3492092



Internal ID18733047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179457255..179490325hg38UCSC Ensembl
Innerchr1:179426390..179459460hg19UCSC Ensembl
Innerchr1:177693013..177726083hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3833071
hg1933071
hg1833071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011557
Supporting Variants
Samples
Known GenesAXDND1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3492092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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