A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998932



Internal ID16945198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6210390..6244089hg38UCSC Ensembl
Outerchr19:6210401..6244100hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3833700
hg1933700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953953
Supporting Variants
SamplesBILGI_BIOE
Known GenesMLLT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998932
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer