A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515500



Internal ID22573462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13896104..13929098hg38UCSC Ensembl
chrX:13914223..13947217hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3832995
hg1932995
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975046
Supporting Variants
Samples
Known GenesGPM6B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515500
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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