A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951665



Internal ID17300539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156166907..156180606hg38UCSC Ensembl
Outerchr7:155959601..155973300hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998642
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951665
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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