A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463571



Internal ID22521457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37323391..37323391hg38UCSC Ensembl
chrX:37182644..37182644hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463571
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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