A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767577



Internal ID19311935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7272166..7273967hg38UCSC Ensembl
chr6:7272399..7274200hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077467
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767577
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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