A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950284



Internal ID16952471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:22142808..22143707hg38UCSC Ensembl
Outerchr1:22469301..22470200hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997094
SamplesBILGI_BIOE
Known GenesWNT4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950284
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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