A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708755



Internal ID21230537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220466558..220466558hg38UCSC Ensembl
chr1:220639900..220639900hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708755
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.903226


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