A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391715



Internal ID21049268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:72402601..72404600hg38UCSC Ensembl
chr4:73268318..73270317hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120183
Samples
Known GenesADAMTS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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