A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355837



Internal ID21013390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32955625..33278452hg38UCSC Ensembl
chr4:32957247..33280074hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38322828
hg19322828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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