A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705822



Internal ID21227623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730209..9730378hg38UCSC Ensembl
chrX:9698249..9698418hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820659
Supporting Variants
Samples
Known GenesGPR143
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705822
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.4375


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