A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401314



Internal ID21058867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74338943..74374234hg38UCSC Ensembl
chr6:75048659..75083950hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3835292
hg1935292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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