A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386237



Internal ID22444107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63668005..63668005hg38UCSC Ensembl
chr17:61745365..61745365hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972882
Supporting Variants
Samples
Known GenesMAP3K3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386237
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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