A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134474



Internal ID21416542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1603968..1603968hg38UCSC Ensembl
chr5:1604083..1604083hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624578
Supporting Variants
SamplesHG00731
Known GenesLOC728613
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134474
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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