A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074138



Internal ID18971432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3765772..3766673hg38UCSC Ensembl
chr4:3767499..3768400hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765118
SamplesKWP1
Known GenesADRA2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074138
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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