A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607060



Internal ID20980131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99270281..99271280hg38UCSC Ensembl
chr6:99718157..99719156hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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