A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997567



Internal ID19157103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75412686..75620267hg38UCSC Ensembl
Innerchr3:75461837..75669418hg19UCSC Ensembl
Innerchr3:75544527..75752108hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38207582
hg19207582
hg18207582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4778n100
Supporting Variantsnssv3733708
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997567
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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