A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772642



Internal ID18964412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156264905..156268506hg38UCSC Ensembl
chr7:156057599..156061200hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383602
hg193602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076632
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772642
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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