A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045158



Internal ID18787689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15034129..15100193hg38UCSC Ensembl
Innerchr16:15127986..15194050hg19UCSC Ensembl
Innerchr16:15035487..15101551hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3866065
hg1966065
hg1866065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2770n100
Supporting Variantsnssv3557955
Samples
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045158
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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