A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473363



Internal ID22531256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74766849..74771948hg38UCSC Ensembl
chr16:74800747..74805846hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879974
Supporting Variants
Samples
Known GenesFA2H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473363
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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