A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610842



Internal ID20983913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143011225..143011924hg38UCSC Ensembl
chr6:143332362..143333061hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140195
Samples
Known GenesLOC100507489
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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