A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769833



Internal ID18963331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79242442..79243543hg38UCSC Ensembl
chr10:81002199..81003300hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070878
Supporting Variants
SamplesKWP1
Known GenesZMIZ1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769833
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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