A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820588



Internal ID21265926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71071575..71071575hg38UCSC Ensembl
chrX:70291425..70291425hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711512
Samples
Known GenesSNX12
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820588
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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