A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516069



Internal ID22574031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2776668..2781649hg38UCSC Ensembl
chrX:2694709..2699690hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg384982
hg194982
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979723
Supporting Variants
Samples
Known GenesXG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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