A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165480



Internal ID21471042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127625450..127752681hg38UCSC Ensembl
chrX:126759431..126886662hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38127232
hg19127232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665124
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165480
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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