A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066136



Internal ID19155355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34962968..35199952hg38UCSC Ensembl
Innerchr16:34197339..34434323hg19UCSC Ensembl
Innerchr16:34054840..34291824hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38236985
hg19236985
hg18236985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556012, nssv3556011, nssv3556010
Samples
Known GenesUBE2MP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066136
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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