A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998929



Internal ID16945195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:4540589..4723488hg38UCSC Ensembl
Outerchr19:4540601..4723500hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38182900
hg19182900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953950
Supporting Variants
SamplesBILGI_BIOE
Known GenesC19orf10, DPP9, LOC100131094, SEMA6B, TNFAIP8L1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998929
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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