A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408127



Internal ID21065680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70523651..70524320hg38UCSC Ensembl
chr6:71233354..71234023hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144451
Samples
Known GenesFAM135A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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