A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048809



Internal ID18791340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110924064..111021655hg38UCSC Ensembl
Innerchr10:112683822..112781413hg19UCSC Ensembl
Innerchr10:112673812..112771403hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3897592
hg1997592
hg1897592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv974n100
Supporting Variantsnssv3519624
Samples
Known GenesRPL13AP6, SHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048809
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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