A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537139



Internal ID20910479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57340518..57350151hg38UCSC Ensembl
chr20:55915574..55925207hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg389634
hg199634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070472
Samples
Known GenesMIR5095, SPO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537139
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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