A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601965



Internal ID20975036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130572501..130576800hg38UCSC Ensembl
chr6:130893646..130897945hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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