A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603988



Internal ID20977059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102682001..102707600hg38UCSC Ensembl
chr6:103129876..103155475hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3825600
hg1925600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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