A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765384



Internal ID18962060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30134783..30135384hg38UCSC Ensembl
chr7:30174399..30175000hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074492
Supporting Variants
SamplesKWP1
Known GenesMTURN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765384
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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