A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15206203



Internal ID21345001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146382747..146382747hg38UCSC Ensembl
chrX:145464265..145464265hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942031
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15206203
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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