A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607202



Internal ID20980273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139775534..139851572hg38UCSC Ensembl
chr6:140096671..140172709hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3876039
hg1976039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138501
Samples
Known GenesLOC100132735
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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