A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167957



Internal ID21484552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74568458..74568585hg38UCSC Ensembl
chrX:73788293..73788420hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665520
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167957
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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