A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583067



Internal ID18881348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176294754..176338618hg38UCSC Ensembl
Innerchr2:177159482..177203346hg19UCSC Ensembl
Innerchr2:176867728..176911592hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3843865
hg1943865
hg1843865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006803
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)nssv3583067
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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