A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156651



Internal ID22087052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23101028..23104578hg38UCSC Ensembl
Outerchr7:23101005..23105676hg38UCSC Ensembl
Innerchr7:23140647..23144197hg19UCSC Ensembl
Outerchr7:23140624..23145295hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384672
hg194672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021061
Samples
Known GenesKLHL7-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156651
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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