A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436953



Internal ID215557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202874552..202874629hg38UCSC Ensembl
chr1:202843680..202843757hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683822
Samples
Known GenesLOC148709
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436953
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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