A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852735



Internal ID15800005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13200753..13206350hg38UCSC Ensembl
Innerchr16:13294610..13300207hg19UCSC Ensembl
Innerchr16:13202111..13207708hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385598
hg195598
hg185598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571490
Supporting Variants
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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