A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138988



Internal ID20706028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139289536..139294172hg38UCSC Ensembl
chr6:139610673..139615309hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg384637
hg194637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611894
Supporting Variants
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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