A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022283



Internal ID19111501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147342405..147379584hg38UCSC Ensembl
Innerchr6:147663541..147700720hg19UCSC Ensembl
Innerchr6:147705234..147742413hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3837180
hg1937180
hg1837180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6160n100
Supporting Variantsnssv3654461
Samples
Known GenesSTXBP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022283
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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