A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932224



Internal ID21352294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148547139..148547216hg38UCSC Ensembl
chrX:147628660..147628737hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200294
SamplesHG002
Known GenesAFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932224
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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