A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201610



Internal ID21340384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173735920..173735920hg38UCSC Ensembl
chr5:173162923..173162923hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935341
Supporting Variants
SamplesHG002
Known GenesLOC101928136
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201610
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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