A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973955



Internal ID22748890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56099508..56135089hg38UCSC Ensembl
chrX:56125941..56161522hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3835582
hg1935582
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973955
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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