A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998591



Internal ID17291543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131585542..131591341hg38UCSC Ensembl
Outerchr7:131270301..131276100hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949950
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998591
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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