A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074770



Internal ID18972303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168693104..168693206hg38UCSC Ensembl
chr4:169614255..169614357hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765931
SamplesKWP1
Known GenesPALLD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074770
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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