A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167971



Internal ID21465703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75556023..75562134hg38UCSC Ensembl
chrX:74775858..74781969hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg386112
hg196112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671041
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167971
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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