A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018084



Internal ID19107301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136216797..136298936hg38UCSC Ensembl
Innerchr7:135901545..135983684hg19UCSC Ensembl
Innerchr7:135552085..135634224hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3882140
hg1982140
hg1882140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6638n100
Supporting Variantsnssv3664234
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)nsv1018084
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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