A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046911



Internal ID19136130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26605419..26680452hg38UCSC Ensembl
Innerchr10:26894348..26969381hg19UCSC Ensembl
Innerchr10:26934354..27009387hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3875034
hg1975034
hg1875034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv694n100
Supporting Variantsnssv3511548, nssv3520697, nssv3510985, nssv3506454, nssv3519846, nssv3506607, nssv3519465, nssv3516648, nssv3522253, nssv3512209, nssv3521823, nssv3507597
Samples
Known GenesLINC00202-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046911
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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