A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025491



Internal ID19114709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:71930623..71992240hg38UCSC Ensembl
Innerchr8:72842858..72904475hg19UCSC Ensembl
Innerchr8:73005412..73067029hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3861618
hg1961618
hg1861618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689524
Samples
Known GenesLOC100132891, RNU6-83P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025491
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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