A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968700



Internal ID22743635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23771961..23784206hg38UCSC Ensembl
chrX:23790078..23802323hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3812246
hg1912246
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516002
Samples
Known GenesSAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968700
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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