A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436735



Internal ID215344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203306116..203306231hg38UCSC Ensembl
chr1:203275244..203275359hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16894875
Samples
Known GenesBTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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