A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400634



Internal ID21058187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95706601..95712200hg38UCSC Ensembl
chr5:95042305..95047904hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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