A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077637



Internal ID19323086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113689859..113689928hg38UCSC Ensembl
Outerchr10:115449618..115449687hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772233
SamplesKWP1
Known GenesCASP7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077637
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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