A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616686



Internal ID20989757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96541201..96542200hg38UCSC Ensembl
chr6:96989077..96990076hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150480
Samples
Known GenesUFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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