A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968332



Internal ID22743268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74847458..74857088hg38UCSC Ensembl
chrX:74067293..74076923hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg389631
hg199631
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516722
Samples
Known GenesKIAA2022
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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