A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710286



Internal ID19008567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:16598736..16661600hg38UCSC Ensembl
Innerchr12:16751670..16814534hg19UCSC Ensembl
Innerchr12:16642937..16705801hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3862865
hg1962865
hg1862865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037740
Supporting Variants
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)nssv3710286
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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