A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025768



Internal ID21935111
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 StatusM
Merged Variants
Supporting Variantsnssv17628178
Samples
Known GenesGRIN2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer