A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956429



Internal ID16958616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87378782..87378941hg38UCSC Ensembl
Outerchr4:88299934..88300093hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005361
SamplesBILGI_BIOE
Known GenesHSD17B11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956429
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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