A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028572



Internal ID19117790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8078321..8234503hg38UCSC Ensembl
Innerchr8:7935843..8092025hg19UCSC Ensembl
Innerchr8:7973253..8129435hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38156183
hg19156183
hg18156183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6995n100
Supporting Variantsnssv3681577
Samples
Known GenesFAM86B3P, MIR548I3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028572
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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