A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934607



Internal ID22709936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74687794..74687950hg38UCSC Ensembl
chr16:74721692..74721848hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377782
Samples
Known GenesMLKL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934607
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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