A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409896



Internal ID22467766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109219736..109219880hg38UCSC Ensembl
chr6:109540939..109541083hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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