A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143485



Internal ID18937691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:134760..135860hg38UCSC Ensembl
Outerchr10:180700..181800hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv328n106
Supporting Variantsnssv3980689
SamplesKWS1
Known GenesZMYND11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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