A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000974



Internal ID17293926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102848250..102848576hg38UCSC Ensembl
Outerchr7:102488697..102489023hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957608
Supporting Variants
SamplesBILGI_BIOE
Known GenesFBXL13
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000974
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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