A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601018



Internal ID20974089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142494125..142621345hg38UCSC Ensembl
chr6:142815262..142942482hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38127221
hg19127221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140154
Samples
Known GenesLOC153910
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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