A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820896



Internal ID21266234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71520413..71521245hg38UCSC Ensembl
chrX:70740263..70741095hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705254
Samples
Known GenesBCYRN1, TAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820896
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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