A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382690



Internal ID21040243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73562707..73563072hg38UCSC Ensembl
chr4:74428424..74428789hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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