A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073879



Internal ID18972549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42628197..42630898hg38UCSC Ensembl
chr5:42628299..42631000hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772782
SamplesKWP1
Known GenesGHR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073879
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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