A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689524



Internal ID18987805
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 StatusS
Merged Variantsnsv1025491
Supporting Variants
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)nssv3689524
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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