A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955670



Internal ID16957857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:76027529..76027756hg38UCSC Ensembl
Outerchr4:76948682..76948909hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005212
SamplesBILGI_BIOE
Known GenesART3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955670
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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