A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052359



Internal ID18794890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46962260hg38UCSC Ensembl
Innerchr10:46590219..47153919hg19UCSC Ensembl
Innerchr10:46010225..46573925hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38566418
hg19563701
hg18563701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv738n100
Supporting Variantsnssv3519188
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, 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)nsv1052359
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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