A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165100



Internal ID21480867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120241384..120241722hg38UCSC Ensembl
chrX:119375237..119375577hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38339
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666309
Supporting Variants
SamplesHG03683
Known GenesNKAPP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165100
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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