A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143639



Internal ID18922606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49964161..49965190hg38UCSC Ensembl
Outerchr10:51269900..51270800hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381030
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994325
SamplesKWS1
Known GenesLOC728407, PARG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143639
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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