A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372649



Internal ID21030202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2504981..2505571hg38UCSC Ensembl
chr4:2506708..2507298hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211790
Samples
Known GenesRNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372649
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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