A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583052



Internal ID18881333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176290690..176337492hg38UCSC Ensembl
Innerchr2:177155418..177202220hg19UCSC Ensembl
Innerchr2:176863664..176910466hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3846803
hg1946803
hg1846803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997276
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)nssv3583052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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