A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123638



Internal ID18910044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:36386417..36386476hg38UCSC Ensembl
Outerchr3:36427909..36427968hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973407
SamplesKWS2
Known GenesSTAC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123638
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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