A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953571



Internal ID17302445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39152861..39222260hg38UCSC Ensembl
Outerchr19:39643501..39712900hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3869400
hg1969400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999837
SamplesBILGI_BIOE
Known GenesNCCRP1, PAK4, SYCN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953571
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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