A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419599



Internal ID22477469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177045909..177229532hg38UCSC Ensembl
chr4:177967063..178150686hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38183624
hg19183624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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