A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027909



Internal ID19117127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8101428..8229622hg38UCSC Ensembl
Innerchr8:7958950..8087144hg19UCSC Ensembl
Innerchr8:7996360..8124554hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38128195
hg19128195
hg18128195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6995n100
Supporting Variantsnssv3681618
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027909
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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