A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401621



Internal ID21059174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156845958..156847946hg38UCSC Ensembl
chr5:156272969..156274957hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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