A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631518



Internal ID21579823
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 StatusM
Merged Variants
Supporting Variantsnssv17142335
SamplesNA19239
Known GenesLAMA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631518
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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