A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628178



Internal ID21820225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74847406..74851940hg38UCSC Ensembl
chr17:72843545..72848079hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384535
hg194535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025768
Supporting Variants
Samples
Known GenesGRIN2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628178
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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