A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195749



Internal ID20762789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91269413..91494168hg38UCSC Ensembl
chr10:93029170..93253925hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38224756
hg19224756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442576
Supporting Variants
Samples
Known GenesHECTD2, LOC100188947, PCGF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195749
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer