A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395881



Internal ID21053434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42839001..42848100hg38UCSC Ensembl
chr6:42806739..42815838hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143392
Samples
Known GenesGLTSCR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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