A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073719



Internal ID19318510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2260372..2262373hg38UCSC Ensembl
chr4:2262099..2264100hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772617
SamplesKWP1
Known GenesMXD4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073719
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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