A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205641



Internal ID21344442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27527977..27527977hg38UCSC Ensembl
chrX:27546094..27546094hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946038
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205641
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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