A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017627



Internal ID19106844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10514522..10740852hg38UCSC Ensembl
Innerchr7:10554149..10780479hg19UCSC Ensembl
Innerchr7:10520674..10747004hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38226331
hg19226331
hg18226331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642911
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)nsv1017627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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