A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956982



Internal ID16959169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:6352597..6376151hg38UCSC Ensembl
Outerchr7:6392228..6415782hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3823555
hg1923555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003645
SamplesBILGI_BIOE
Known GenesRAC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956982
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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