A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571485



Internal ID16012208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13200753..13202182hg38UCSC Ensembl
Innerchr16:13294610..13296039hg19UCSC Ensembl
Innerchr16:13202111..13203540hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381430
hg191430
hg181430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4913n54
Supporting Variantsnssv852564, nssv852559, nssv852566, nssv852563, nssv852562, nssv852558, nssv852561, nssv852565, nssv852557, nssv852560
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571485
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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