A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625648



Internal ID21817695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18358223..18358984hg38UCSC Ensembl
chr17:18261537..18262298hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030832
Supporting Variants
Samples
Known GenesSHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625648
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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