A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074808



Internal ID19320689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8026910..8027213hg38UCSC Ensembl
chr5:8027023..8027326hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762822
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074808
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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