A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767593



Internal ID19311389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17042285..17042886hg38UCSC Ensembl
chr17:16945599..16946200hg19UCSC 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 Variantsnsv1070816
Supporting Variants
SamplesKWP1
Known GenesMPRIP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767593
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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