A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997902



Internal ID19157438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36580172..36641313hg38UCSC Ensembl
Innerchr3:36621664..36682805hg19UCSC Ensembl
Innerchr3:36596668..36657809hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3861142
hg1961142
hg1861142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4720n100
Supporting Variantsnssv3589661
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)nsv997902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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