A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996729



Internal ID16942995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74415384..74456483hg38UCSC Ensembl
Outerchr4:75281101..75322200hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3841100
hg1941100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950052
Supporting Variants
SamplesBILGI_BIOE
Known GenesAREG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996729
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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