A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029266



Internal ID19118485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47139967..47186991hg38UCSC Ensembl
Innerchr7:47179565..47226589hg19UCSC Ensembl
Innerchr7:47146090..47193114hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3847025
hg1947025
hg1847025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661242
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)nsv1029266
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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