A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383604



Internal ID21041157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97448793..97519428hg38UCSC Ensembl
chr4:98369944..98440579hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3870636
hg1970636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214386
Samples
Known GenesSTPG2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383604
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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