A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583460



Internal ID21775503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101595257..101595257hg38UCSC Ensembl
chr8:102607485..102607485hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065379
Supporting Variants
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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