A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766067



Internal ID18959607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56843401..56844102hg38UCSC Ensembl
chr6:56708199..56708900hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073561
Supporting Variants
SamplesKWP1
Known GenesDST
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766067
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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