A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977788



Internal ID22752723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23996395..24003221hg38UCSC Ensembl
chrX:24014512..24021338hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg386827
hg196827
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516009
Samples
Known GenesKLHL15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977788
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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