A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619468



Internal ID20992539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136830548..136834270hg38UCSC Ensembl
chr6:137151686..137155408hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg383723
hg193723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138311
Samples
Known GenesPEX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619468
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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