A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949782



Internal ID16951969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8033474..8035073hg38UCSC Ensembl
Outerchr4:8035201..8036800hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996654
SamplesBILGI_BIOE
Known GenesABLIM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949782
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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