A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616084



Internal ID20989155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134220349..134223358hg38UCSC Ensembl
chr6:134541487..134544496hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383010
hg193010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139418
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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