A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143518



Internal ID18918344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112455141..112455441hg38UCSC Ensembl
Outerchr10:114214900..114215200hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980724
SamplesKWS1
Known GenesVTI1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143518
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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