A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603775



Internal ID20976846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139235568..139245115hg38UCSC Ensembl
chr6:139556705..139566252hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg389548
hg199548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138422
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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