A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433830



Internal ID212531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13761805..13761904hg38UCSC Ensembl
chrX:13779924..13780023hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739332
Samples
Known GenesOFD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433830
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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