A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998084



Internal ID19157621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36590547..36641313hg38UCSC Ensembl
Innerchr3:36632039..36682805hg19UCSC Ensembl
Innerchr3:36607043..36657809hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3850767
hg1950767
hg1850767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4720n100
Supporting Variantsnssv3589668, nssv3589670, nssv3589664, nssv3589665, nssv3589666, nssv3589669, nssv3589667
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998084
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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