A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387598



Internal ID21045151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73201530..73266614hg38UCSC Ensembl
chr4:74067247..74132331hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3865085
hg1965085
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212345
Samples
Known GenesANKRD17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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