A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819412



Internal ID21264751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100853424..100853424hg38UCSC Ensembl
chrX:100108413..100108413hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707134
Samples
Known GenesNOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819412
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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