A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224660



Internal ID22368020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9585492..9585639hg38UCSC Ensembl
chr17:9488809..9488956hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383158, nssv14375578, nssv14379960
SamplesNA19238, NA19239, NA19240
Known GenesWDR16
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224660
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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