A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989717



Internal ID19240908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:21533771..21535271hg38UCSC Ensembl
Outerchr10:21822700..21824200hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136112
Supporting Variants
SamplesKWS2
Known GenesMLLT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989717
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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