A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799151



Internal ID21244489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44546228..44546890hg38UCSC Ensembl
chrX:49731206..49731799hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38663
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689066
Samples
Known GenesCLCN5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799151
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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