A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770048



Internal ID18960647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162458114..162458289hg38UCSC Ensembl
chr6:162879146..162879321hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074974
Supporting Variants
SamplesKWP1
Known GenesPARK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770048
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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