A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951684



Internal ID16953871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:159006110..159037209hg38UCSC Ensembl
Outerchr7:158798801..158829900hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3831100
hg1931100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998661
SamplesBILGI_BIOE
Known GenesLINC00689, VIPR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951684
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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