A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956973



Internal ID17305846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:114075869..114077922hg38UCSC Ensembl
Outerchr7:113715924..113717977hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000934
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956973
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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