A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800870



Internal ID21246208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150990243..150990243hg38UCSC Ensembl
chr1:150962719..150962719hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691538
Samples
Known GenesANXA9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800870
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