A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398142



Internal ID21055695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56674314..56675372hg38UCSC Ensembl
chr5:55970141..55971199hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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