A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019518



Internal ID19108736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105911241..105946847hg38UCSC Ensembl
Innerchr8:106923469..106959075hg19UCSC Ensembl
Innerchr8:106992645..107028251hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3835607
hg1935607
hg1835607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691264, nssv3691265, nssv3691266, nssv3691267
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)nsv1019518
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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