A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956525



Internal ID17305398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:4050026..4050319hg38UCSC Ensembl
Outerchr6:4050260..4050553hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003434
SamplesBILGI_BIOE
Known GenesPRPF4B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956525
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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