A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410181



Internal ID21067734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133031771..133040537hg38UCSC Ensembl
chr5:132367463..132376229hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg388767
hg198767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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