A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165990



Internal ID21480763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19447897..19451499hg38UCSC Ensembl
chrX:19466015..19469617hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg383603
hg193603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671679
Supporting Variants
SamplesHG03683
Known GenesMAP3K15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165990
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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