A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165164



Internal ID21511687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139536239..139536239hg38UCSC Ensembl
chrX:138618398..138618398hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620075
Supporting Variants
SamplesNA24385
Known GenesF9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165164
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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