A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999791



Internal ID16946057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:22598099..22629098hg38UCSC Ensembl
Outerchr19:22780901..22811900hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3831000
hg1931000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953255
Supporting Variants
SamplesBILGI_BIOE
Known GenesLOC100996349, LOC440518
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999791
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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