A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034963



Internal ID18777495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1596259..1733615hg38UCSC Ensembl
Innerchr8:1544425..1681781hg19UCSC Ensembl
Innerchr8:1531832..1669188hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38137357
hg19137357
hg18137357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675058
Samples
Known GenesDLGAP2, LOC100507435
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034963
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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