A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762950



Internal ID20538810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74325022..74325089hg38UCSC Ensembl
chrX:73544857..73544924hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762950
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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