A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140875



Internal ID19273543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:157481688..157481758hg38UCSC Ensembl
Outerchr7:157274382..157274452hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992376
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140875
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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