A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036899



Internal ID19126118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7862523..7929135hg38UCSC Ensembl
Innerchr16:7912525..7979137hg19UCSC Ensembl
Innerchr16:7852526..7919138hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3866613
hg1966613
hg1866613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2721n100
Supporting Variantsnssv3557093
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)nsv1036899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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