A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619644



Internal ID20992715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138727539..138728402hg38UCSC Ensembl
chr6:139048676..139049539hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138401
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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