A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149274



Internal ID15855012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:383623..445662hg38UCSC Ensembl
Innerchr16:433623..495662hg19UCSC Ensembl
Innerchr16:373624..435663hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3862040
hg1962040
hg1862040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570958
Supporting Variants
Samples1780862415_A
Known GenesDECR2, LOC100134368, NME4, RAB11FIP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149274
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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