A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905910



Internal ID22681103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81967247..81969895hg38UCSC Ensembl
chr6:82676964..82679612hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905910
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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