A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165656



Internal ID21403596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129186509..129193582hg38UCSC Ensembl
chrX:128320486..128327559hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg387074
hg197074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666720
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165656
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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