A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167967



Internal ID21485920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75334611..75334803hg38UCSC Ensembl
chrX:74554446..74554638hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670178
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167967
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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