A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749556



Internal ID19047837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144146928..144181687hg38UCSC Ensembl
Innerchr6:144468065..144502824hg19UCSC Ensembl
Innerchr6:144509758..144544517hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3834760
hg1934760
hg1834760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024333
Supporting Variants
Samples
Known GenesSTX11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749556
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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