A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044706



Internal ID18787237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12967718..13004583hg38UCSC Ensembl
Innerchr16:13061575..13098440hg19UCSC Ensembl
Innerchr16:12969076..13005941hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3836866
hg1936866
hg1836866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718888
Samples
Known GenesSHISA9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044706
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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