A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820406



Internal ID21265744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53967177..53967177hg38UCSC Ensembl
chrX:53993610..53993610hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709127
Samples
Known GenesPHF8
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820406
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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