A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953945



Internal ID17302819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:2555403..2561602hg38UCSC Ensembl
Outerchr19:2555401..2561600hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998924
SamplesBILGI_BIOE
Known GenesGNG7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953945
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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