A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322993



Internal ID20856108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156117202..156207324hg38UCSC Ensembl
chr1:156086993..156177115hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3890123
hg1990123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200921
Samples
Known GenesLMNA, MIR7851, SEMA4A, SLC25A44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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