A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026255



Internal ID18768787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140244673..140343499hg38UCSC Ensembl
Innerchr7:139944473..140043299hg19UCSC Ensembl
Innerchr7:139590942..139689768hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3898827
hg1998827
hg1898827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664249
Samples
Known GenesSLC37A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026255
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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