A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613729



Internal ID20986800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148096742..148097162hg38UCSC Ensembl
chr6:148417878..148418298hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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