A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515096



Internal ID22573055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10708712..10730723hg38UCSC Ensembl
chrX:10676752..10698763hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3822012
hg1922012
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968329
Supporting Variants
Samples
Known GenesMID1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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