A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037881



Internal ID18780412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:16388577..16677394hg38UCSC Ensembl
Innerchr12:16541511..16830328hg19UCSC Ensembl
Innerchr12:16432778..16721595hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38288818
hg19288818
hg18288818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504390
Samples
Known GenesLMO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037881
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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