A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017114



Internal ID19106331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108051958..108079717hg38UCSC Ensembl
Innerchr7:107692403..107720162hg19UCSC Ensembl
Innerchr7:107479639..107507398hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3827760
hg1927760
hg1827760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656219
Samples
Known GenesLAMB4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017114
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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