A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168137



Internal ID21479761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68894609..68894677hg38UCSC Ensembl
chrX:68114452..68114520hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666576
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168137
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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