A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953586



Internal ID17302460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:42788149..43043148hg38UCSC Ensembl
Outerchr19:43292301..43547300hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38255000
hg19255000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999852
SamplesBILGI_BIOE
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953586
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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