A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619018



Internal ID20992089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113179622..113179778hg38UCSC Ensembl
chr6:113500824..113500980hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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