A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583064



Internal ID18881345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176292655..176360770hg38UCSC Ensembl
Innerchr2:177157383..177225498hg19UCSC Ensembl
Innerchr2:176865629..176933744hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3868116
hg1968116
hg1868116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008093
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)nssv3583064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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