A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072717



Internal ID18975118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141486257..141487658hg38UCSC Ensembl
chr3:141205099..141206500hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772324
SamplesKWP1
Known GenesRASA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072717
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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