A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999874



Internal ID16946140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:51689148..51704247hg38UCSC Ensembl
Outerchr19:52192401..52207500hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3815100
hg1915100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953608
Supporting Variants
SamplesBILGI_BIOE
Known GenesMIR125A, MIR99B, MIRLET7E, SPACA6P, SPACA6P-AS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999874
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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