A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022912



Internal ID18765446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:46125672..46148712hg38UCSC Ensembl
Innerchr6:46093409..46116449hg19UCSC Ensembl
Innerchr6:46201368..46224408hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3823041
hg1923041
hg1823041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657443
Samples
Known GenesENPP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022912
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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