A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767919



Internal ID19305386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15129250..15129312hg38UCSC Ensembl
chr7:15168875..15168937hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075012
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767919
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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