A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943812



Internal ID22719267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61224757..61314213hg38UCSC Ensembl
chr16:61258661..61348117hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3889457
hg1989457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943812
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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