A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400672



Internal ID21058225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132181417..132190082hg38UCSC Ensembl
chr5:131517110..131525775hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg388666
hg198666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127119
Samples
Known GenesP4HA2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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