A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473361



Internal ID22531254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74670413..74672212hg38UCSC Ensembl
chr16:74704311..74706110hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879333
Supporting Variants
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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