A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546964



Internal ID21871319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102171232..102171232hg38UCSC Ensembl
chr4:103092389..103092389hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546964
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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