A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011756



Internal ID19100974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75489692..75732546hg38UCSC Ensembl
Innerchr3:75538843..75781697hg19UCSC Ensembl
Innerchr3:75621533..75864387hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38242855
hg19242855
hg18242855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4790n100
Supporting Variantsnssv3733753
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011756
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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