A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023772



Internal ID18766305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86165139..86321965hg38UCSC Ensembl
Innerchr8:87177368..87334194hg19UCSC Ensembl
Innerchr8:87246484..87403310hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38156827
hg19156827
hg18156827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7263n100
Supporting Variantsnssv3689679
Samples
Known GenesSLC7A13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023772
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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