A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029841



Internal ID19119060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119659573..119966578hg38UCSC Ensembl
Innerchr7:119299627..119606632hg19UCSC Ensembl
Innerchr7:119086863..119393868hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38307006
hg19307006
hg18307006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6598n100
Supporting Variantsnssv3662083
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)nsv1029841
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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