A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574375



Internal ID21766418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112239352..112239352hg38UCSC Ensembl
chr6:112560553..112560553hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073084
Supporting Variants
Samples
Known GenesLAMA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574375
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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