A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977218



Internal ID22752153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24092921..24098749hg38UCSC Ensembl
chrX:24111038..24116866hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385829
hg195829
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977218
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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