A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010580



Internal ID19099797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77944516..77979170hg38UCSC Ensembl
Innerchr2:78171642..78206296hg19UCSC Ensembl
Innerchr2:78025150..78059804hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3834655
hg1934655
hg1834655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731999
Samples
Known GenesSNAR-H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010580
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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