A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951448



Internal ID17300322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:80873266..80874665hg38UCSC Ensembl
Outerchr8:81785501..81786900hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999301
SamplesBILGI_BIOE
Known GenesZNF704
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951448
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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