A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035848



Internal ID19125067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13718833..13767949hg38UCSC Ensembl
Innerchr16:13812690..13861806hg19UCSC Ensembl
Innerchr16:13720191..13769307hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3849117
hg1949117
hg1849117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557233, nssv3557232
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)nsv1035848
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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