A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533983



Internal ID21858339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121397857..121408624hg38UCSC Ensembl
chr1:121139717..121150484hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg3810768
hg1910768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980952
Supporting Variants
Samples
Known GenesSRGAP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533983
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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