A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767661



Internal ID18959497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59882414..59882598hg38UCSC Ensembl
chr10:61642172..61642356hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069054
Supporting Variants
SamplesKWP1
Known GenesCCDC6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767661
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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