A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994311



Internal ID19216717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:21534071..21535071hg38UCSC Ensembl
Outerchr10:21823000..21824000hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143625
Supporting Variants
SamplesKWS1
Known GenesMLLT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994311
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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