A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377557



Internal ID22435427
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 StatusS
Merged Variantsnsv5943812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377557
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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