A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026896



Internal ID18769427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71538477..72256531hg38UCSC Ensembl
Innerchr7:71003462..71721516hg19UCSC Ensembl
Innerchr7:70641398..71359452hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38718055
hg19718055
hg18718055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655693
Samples
Known GenesCALN1, WBSCR17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026896
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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