A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355805



Internal ID21013358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33737795..33761955hg38UCSC Ensembl
chr4:33739417..33763577hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3824161
hg1924161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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