A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139097



Internal ID18906778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:16317771..16317834hg38UCSC Ensembl
Outerchr3:16359278..16359341hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991721
SamplesKWS2
Known GenesRFTN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139097
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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