A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018179



Internal ID19107396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126403590..126422954hg38UCSC Ensembl
Innerchr7:126043644..126063008hg19UCSC Ensembl
Innerchr7:125830880..125850244hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3819365
hg1919365
hg1819365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6614n100
Supporting Variantsnssv3662168
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)nsv1018179
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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