A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998568



Internal ID16944834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107890656..107915255hg38UCSC Ensembl
Outerchr7:107531101..107555700hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3824600
hg1924600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949927
Supporting Variants
SamplesBILGI_BIOE
Known GenesDLD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998568
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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