A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191702



Internal ID21330564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101976000..101976000hg38UCSC Ensembl
chr10:103735757..103735757hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945916
Supporting Variants
SamplesHG002
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191702
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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