A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767964



Internal ID19308264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21042886..21043487hg38UCSC Ensembl
chr17:20946199..20946800hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072726
Supporting Variants
SamplesKWP1
Known GenesUSP22
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767964
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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