A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952906



Internal ID16955093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:2868600..3028099hg38UCSC Ensembl
Outerchr16:2918601..3078100hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38159500
hg19159500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999202
SamplesBILGI_BIOE
Known GenesCCDC64B, CLDN6, CLDN9, FLYWCH1, FLYWCH2, HCFC1R1, KREMEN2, LINC00514, PAQR4, PKMYT1, THOC6, TNFRSF12A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952906
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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