A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896731



Internal ID22671826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81048638..81400548hg38UCSC Ensembl
chr6:81758355..82110265hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38351911
hg19351911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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