A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609969



Internal ID20983040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131589722..131590289hg38UCSC Ensembl
chr6:131910862..131911429hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139646
Samples
Known GenesMED23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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