A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036503



Internal ID19125722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121675623..121696088hg38UCSC Ensembl
Innerchr10:123435137..123455602hg19UCSC Ensembl
Innerchr10:123425127..123445592hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3820466
hg1920466
hg1820466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv984n100
Supporting Variantsnssv3706247, nssv3706249, nssv3706246, nssv3706248, nssv3517436
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036503
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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