A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950819



Internal ID17299693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:25844281..25849980hg38UCSC Ensembl
Outerchr7:25883901..25889600hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997623
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950819
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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