A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142335



Internal ID21500098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112210865..112210865hg38UCSC Ensembl
chr6:112532066..112532066hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631518
Supporting Variants
SamplesNA19239
Known GenesLAMA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142335
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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