A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956576



Internal ID17305449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19723638..19728832hg38UCSC Ensembl
Outerchr19:19834447..19839641hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385195
hg195195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv80n73
Supporting Variantsnssv3002827
SamplesBILGI_BIOE
Known GenesZNF14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956576
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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