A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491355



Internal ID19078996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7362646..7530260hg38UCSC Ensembl
Innerchr10:7404608..7572222hg19UCSC Ensembl
Innerchr10:7444614..7612228hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38167615
hg19167615
hg18167615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047356
Supporting Variants
Samples
Known GenesSFMBT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3491355
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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