A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109534



Internal ID19254656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99886216..99886269hg38UCSC Ensembl
Outerchr3:99605060..99605113hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957022
SamplesKWS1
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109534
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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