A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601498



Internal ID20974569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108456101..108458300hg38UCSC Ensembl
chr6:108777304..108779503hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136996
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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