A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583055



Internal ID18881336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176290690..176341108hg38UCSC Ensembl
Innerchr2:177155418..177205836hg19UCSC Ensembl
Innerchr2:176863664..176914082hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3850419
hg1950419
hg1850419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010740
Supporting Variants
Samples
Known GenesMTX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583055
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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