A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167877



Internal ID21484295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56869574..56871093hg38UCSC Ensembl
chrX:56896007..56897526hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg381520
hg191520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666681
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167877
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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