A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036909



Internal ID19126128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46247355..46996235hg19UCSC Ensembl
Innerchr10:45567361..46416241hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg19748881
hg18848881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv731n100
Supporting Variantsnssv3505588
Samples
Known GenesAGAP4, BMS1P1, BMS1P5, FAM21C, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036909
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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