A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949915



Internal ID17298789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101629521..101631820hg38UCSC Ensembl
Outerchr7:101272801..101275100hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998556
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949915
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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