A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143625



Internal ID19283957
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 StatusM
Merged Variants
Supporting Variantsnssv3994311
SamplesKWS1
Known GenesMLLT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143625
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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