A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951578



Internal ID21371648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55720145..55720208hg38UCSC Ensembl
chr3:55754173..55754236hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178995
SamplesHG002
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951578
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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