A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122420



Internal ID19278490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:177663527..177667625hg38UCSC Ensembl
Outerchr3:177381315..177385413hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384099
hg194099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2641n106
Supporting Variantsnssv3970628
SamplesKWS1
Known GenesLINC00578
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122420
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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