A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029455



Internal ID19118674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21175674..21194133hg38UCSC Ensembl
Innerchr7:21215293..21233752hg19UCSC Ensembl
Innerchr7:21181818..21200277hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3818460
hg1918460
hg1818460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643270
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)nsv1029455
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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