A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448155



Internal ID22506025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81760498..81760498hg38UCSC Ensembl
chr6:82470215..82470215hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966878
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448155
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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