A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893644



Internal ID22668707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56461618..56463349hg38UCSC Ensembl
chr6:56326416..56328147hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381732
hg191732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433093
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893644
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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