A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490971



Internal ID18731926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179147966..179159541hg38UCSC Ensembl
Innerchr1:179117101..179128676hg19UCSC Ensembl
Innerchr1:177383724..177395299hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3811576
hg1911576
hg1811576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011210
Supporting Variants
Samples
Known GenesABL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3490971
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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