A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958378



Internal ID16960566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161552389..161552456hg38UCSC Ensembl
Outerchr6:161973421..161973488hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003602
SamplesBILGI_BIOE
Known GenesPARK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958378
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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