A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376723



Internal ID21034276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71597234..71599832hg38UCSC Ensembl
chr4:72462951..72465549hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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