A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029297



Internal ID19118516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:47556273..47618241hg38UCSC Ensembl
Innerchr8:48468835..48530803hg19UCSC Ensembl
Innerchr8:48631388..48693356hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3861969
hg1961969
hg1861969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7212n100
Supporting Variantsnssv3687462
Samples
Known GenesSPIDR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029297
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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