A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610312



Internal ID20983383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108483858..108488052hg38UCSC Ensembl
chr6:108805061..108809255hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384195
hg194195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136999
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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