A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135769



Internal ID18920725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14708905..14708979hg38UCSC Ensembl
Outerchr10:14750904..14750978hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989356
SamplesKWS2
Known GenesFAM107B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135769
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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