A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670630



Internal ID21618935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3823830..3900671hg38UCSC Ensembl
chrX:3741871..3818712hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3876842
hg1976842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167358
SamplesHG00731
Known GenesLOC389906
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670630
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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