A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998587



Internal ID16944853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:129762961..129810560hg38UCSC Ensembl
Outerchr7:129402801..129450400hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3847600
hg1947600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949946
Supporting Variants
SamplesBILGI_BIOE
Known GenesMIR182, MIR183, MIR96
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998587
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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