A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515979



Internal ID20889340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39345201..39346900hg38UCSC Ensembl
chr20:37973844..37975543hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202256, nssv18068891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515979
Frequency
Sample Size19652
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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