A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029362



Internal ID19118581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13639878..13694022hg38UCSC Ensembl
Innerchr7:13679503..13733647hg19UCSC Ensembl
Innerchr7:13646028..13700172hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3854145
hg1954145
hg1854145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643141
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029362
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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