A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154584



Internal ID20721624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43932601..43934800hg38UCSC Ensembl
chr7:43972200..43974399hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607216
Supporting Variants
Samples
Known GenesUBE2D4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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