A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537591



Internal ID20910926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62683919..62735089hg38UCSC Ensembl
chr20:61315271..61366441hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3851171
hg1951171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068551
Samples
Known GenesNTSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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