A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949996



Internal ID16952183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:141306802..141672500hg38UCSC Ensembl
Outerchr8:142316901..142682600hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38365699
hg19365700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999336
SamplesBILGI_BIOE
Known GenesGPR20, LOC731779, MROH5, PTP4A3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949996
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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