A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700162



Internal ID21221996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134959696..134959696hg38UCSC Ensembl
chrX:134093726..134093726hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819786
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700162
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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