A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074232



Internal ID19322472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39374535..39529881hg38UCSC Ensembl
chr8:39232054..39387400hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155347
hg19155347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763535
SamplesKWP1
Known GenesADAM3A, ADAM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074232
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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