A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032053



Internal ID19121275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6376049..6393413hg38UCSC Ensembl
Innerchr8:6233570..6250934hg19UCSC Ensembl
Innerchr8:6220978..6238342hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3817365
hg1917365
hg1817365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6875n100
Supporting Variantsnssv3677425
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032053
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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