A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200009



Internal ID21338805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119796374..119796374hg38UCSC Ensembl
chr4:120717529..120717529hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926610
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200009
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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