A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430851



Internal ID209645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70302444..70302751hg38UCSC Ensembl
chr1:70768127..70768434hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16904090
Samples
Known GenesANKRD13C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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