A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192096



Internal ID21330971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70554970..70554970hg38UCSC Ensembl
chr10:72314726..72314726hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938728
Supporting Variants
SamplesHG002
Known GenesPALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192096
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