A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619593



Internal ID20992664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145827308..145837937hg38UCSC Ensembl
chr6:146148444..146159073hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3810630
hg1910630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140977
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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