A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956428



Internal ID16958615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:271415..271530hg38UCSC Ensembl
Outerchr4:265204..265319hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005355
SamplesBILGI_BIOE
Known GenesZNF732
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956428
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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