A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999604



Internal ID19159141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112115902..112154756hg38UCSC Ensembl
Innerchr1:112658524..112697378hg19UCSC Ensembl
Innerchr1:112460047..112498901hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3838855
hg1938855
hg1838855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv282n100
Supporting Variantsnssv3483552
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)nsv999604
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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