A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046039



Internal ID19135258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8084931..8171974hg38UCSC Ensembl
Innerchr16:8134933..8221976hg19UCSC Ensembl
Innerchr16:8074934..8161977hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3887044
hg1987044
hg1887044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2724n100
Supporting Variantsnssv3557100
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)nsv1046039
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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