A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065103



Internal ID19154322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57817476..57878979hg38UCSC Ensembl
Innerchr16:57851380..57912883hg19UCSC Ensembl
Innerchr16:56408881..56470384hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3861504
hg1961504
hg1861504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559354
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)nsv1065103
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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