A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976526



Internal ID22751461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66929695..66953037hg38UCSC Ensembl
chrX:66149537..66172879hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3823343
hg1923343
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976526
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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