A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719253



Internal ID19017534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934316..19959484hg38UCSC Ensembl
Innerchr16:19945638..19970806hg19UCSC Ensembl
Innerchr16:19853139..19878307hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3825169
hg1925169
hg1825169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040765
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3719253
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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