A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150136



Internal ID19196411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:70548709..70548786hg38UCSC Ensembl
Outerchr10:72308465..72308542hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003440
SamplesKWB1
Known GenesPALD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150136
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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