A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130869



Internal ID19260717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:140871098..140871240hg38UCSC Ensembl
Outerchr7:140570898..140571040hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967570
SamplesKWS2
Known GenesBRAF
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130869
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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