A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999835



Internal ID17292787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38697761..38729860hg38UCSC Ensembl
Outerchr19:39188401..39220500hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3832100
hg1932100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953299
Supporting Variants
SamplesBILGI_BIOE
Known GenesACTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999835
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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