A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690512



Internal ID21212371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103768597..103768597hg38UCSC Ensembl
chr12:104162375..104162375hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690512
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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