A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021061



Internal ID22082692
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156651
Supporting Variants
Samples
Known GenesKLHL7-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021061
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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