A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896801



Internal ID22671897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78678098..78760238hg38UCSC Ensembl
chr6:79387815..79469955hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3882141
hg1982141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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