A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139088



Internal ID19274711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:10047812..10047869hg38UCSC Ensembl
Outerchr3:10089496..10089553hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973391, nssv3956957
SamplesKWS2, KWS1
Known GenesFANCD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139088
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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