A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820263



Internal ID21265601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151743029..151743029hg38UCSC Ensembl
chrX:150911501..150911501hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705040
Samples
Known GenesCNGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820263
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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