A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167558



Internal ID21484732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37008546..37008546hg38UCSC Ensembl
chrX:37026619..37026619hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624319
Supporting Variants
SamplesNA12329
Known GenesFAM47C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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