A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601015



Internal ID20974086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108759901..108762200hg38UCSC Ensembl
chr6:109081104..109083403hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137008
Samples
Known GenesLINC00222
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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