A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073775



Internal ID18978958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77074746..77076047hg38UCSC Ensembl
chr4:77995899..77997200hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772846
SamplesKWP1
Known GenesCCNI
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073775
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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