A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144229



Internal ID19252139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:86342671..86342971hg38UCSC Ensembl
Outerchr8:87354900..87355200hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994961
SamplesKWS1
Known GenesWWP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144229
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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