A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675058



Internal ID18626653
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 StatusS
Merged Variantsnsv1034963
Supporting Variants
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)nssv3675058
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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