A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954838



Internal ID16957025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:218865779..218887278hg38UCSC Ensembl
Outerchr2:219730501..219752000hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3821500
hg1921500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003121
SamplesBILGI_BIOE
Known GenesWNT10A, WNT6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954838
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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