A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818858



Internal ID21264196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23759724..23759724hg38UCSC Ensembl
chrX:23777841..23777841hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818858
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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