A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950797



Internal ID16952984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:4749070..4811369hg38UCSC Ensembl
Outerchr7:4788701..4851000hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3862300
hg1962300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997601
SamplesBILGI_BIOE
Known GenesAP5Z1, FOXK1, MIR4656, RADIL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950797
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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