A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768143



Internal ID19312832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140061799..140063100hg38UCSC Ensembl
chr7:139761599..139762900hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076005
Supporting Variants
SamplesKWP1
Known GenesPARP12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768143
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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