A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952094



Internal ID17300968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:948861..949660hg38UCSC Ensembl
Outerchr17:852101..852900hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000213
SamplesBILGI_BIOE
Known GenesNXN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952094
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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