A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612548



Internal ID20985619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132131012..132132128hg38UCSC Ensembl
chr6:132452152..132453268hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612548
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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