A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954339



Internal ID21374409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42285662..42285662hg38UCSC Ensembl
chrX:42144914..42144914hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205679
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954339
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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