A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820713



Internal ID21266051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39776531..39776654hg38UCSC Ensembl
chrX:39635785..39635908hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820713
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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