A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611444



Internal ID20984515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99846300..99858973hg38UCSC Ensembl
chr6:100294176..100306849hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3812674
hg1912674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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