A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516995



Internal ID22574958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97555922..97564921hg38UCSC Ensembl
chrX:96810921..96819920hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976429
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516995
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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