A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025727



Internal ID18768259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2898667..3024374hg38UCSC Ensembl
Innerchr7:2938301..3064008hg19UCSC Ensembl
Innerchr7:2904827..3030534hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38125708
hg19125708
hg18125708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752789
Samples
Known GenesCARD11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025727
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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