A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701529



Internal ID21223354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47148587..47148648hg38UCSC Ensembl
chrX:47007986..47008047hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820511
Supporting Variants
Samples
Known GenesRBM10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701529
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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