A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377900



Internal ID22435770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63672102..63674385hg38UCSC Ensembl
chr17:61749462..61751745hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg382284
hg192284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929218
Supporting Variants
Samples
Known GenesMAP3K3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377900
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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