A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392603



Internal ID21383633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112148899..112149104hg38UCSC Ensembl
chr6:112470101..112470306hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703906
Samples
Known GenesLAMA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392603
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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