A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953295



Internal ID17302169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:37548399..37552098hg38UCSC Ensembl
Outerchr19:38039301..38043000hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999831
SamplesBILGI_BIOE
Known GenesZNF540, ZNF571-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953295
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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