A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950780



Internal ID17299654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:325335..381734hg38UCSC Ensembl
Outerchr7:365301..421700hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3856400
hg1956400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997584
SamplesBILGI_BIOE
Known GenesLOC442497
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950780
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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