A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003600



Internal ID19092818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119023676..119099194hg38UCSC Ensembl
Innerchr3:118742523..118818041hg19UCSC Ensembl
Innerchr3:120225213..120300731hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3875519
hg1975519
hg1875519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4844n100
Supporting Variantsnssv3735282, nssv3735281, nssv3604508, nssv3604509
Samples
Known GenesIGSF11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003600
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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