A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134046



Internal ID18923484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97054052..97054105hg38UCSC Ensembl
Outerchr10:98813809..98813862hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983100, nssv3970761
SamplesKWS1, KWS2
Known GenesSLIT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134046
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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