A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764967



Internal ID18959987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162327476..162327650hg38UCSC Ensembl
chr6:162748508..162748682hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074032
Supporting Variants
SamplesKWP1
Known GenesPARK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764967
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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