A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767654



Internal ID19310045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21717270..21717971hg38UCSC Ensembl
chr10:22006199..22006900hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069030
Supporting Variants
SamplesKWP1
Known GenesMLLT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767654
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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