A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804007



Internal ID21249345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:7631072..7632596hg38UCSC Ensembl
chr7_gl000195_random:4609..6133hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381525
hg191525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804007
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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