A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568875



Internal ID21760918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73707822..73708151hg38UCSC Ensembl
chr7:73122152..73122481hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017844
Supporting Variants
Samples
Known GenesSTX1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568875
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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