A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040765



Internal ID19129984
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 StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3546894, nssv3719253, nssv3546895
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)nsv1040765
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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