A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977464



Internal ID22752399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72727692..72742140hg38UCSC Ensembl
chrX:71947517..71961963hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3814449
hg1914447
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977464
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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