A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052860



Internal ID18795391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46861290hg38UCSC Ensembl
Innerchr10:46691159..47047587hg19UCSC Ensembl
Innerchr10:46111165..46467593hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38334778
hg19356429
hg18356429
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv740n100
Supporting Variantsnssv3508201, nssv3512668, nssv3512310, nssv3507404, nssv3520826, nssv3522685, nssv3511060, nssv3503071
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052860
Frequency
Sample Size29084
Observed Gain5
Observed Loss3
Observed Complex0
Frequencyn/a


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