A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156697



Internal ID22087098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91400153..91402419hg38UCSC Ensembl
Outerchr7:91397933..91402629hg38UCSC Ensembl
Innerchr7:91029468..91031734hg19UCSC Ensembl
Outerchr7:91027248..91031944hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg384697
hg194697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022166
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156697
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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