A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132140



Internal ID19276093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39158240..39158301hg38UCSC Ensembl
Outerchr8:39015759..39015820hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986833
SamplesKWS1
Known GenesADAM32
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132140
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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