A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037892



Internal ID18780423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21401070..21586942hg38UCSC Ensembl
Innerchr16:21412391..21598263hg19UCSC Ensembl
Innerchr16:21319892..21505764hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38185873
hg19185873
hg18185873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2801n100
Supporting Variantsnssv3548061
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037892
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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