A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706257



Internal ID18657852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130334322..133158679hg38UCSC Ensembl
Innerchr10:132132586..134972183hg19UCSC Ensembl
Innerchr10:132022576..134822173hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382824358
hg192839598
hg182799598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054934
Supporting Variants
Samples
Known GenesBNIP3, C10orf91, DPYSL4, FLJ46300, GPR123, INPP5A, JAKMIP3, LOC399829, LRRC27, MIR378C, NKX6-2, PPP2R2D, PWWP2B, STK32C, TCERG1L, TTC40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706257
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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