A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953888



Internal ID16956075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:37726610..37734411hg38UCSC Ensembl
Outerchr17:36086601..36094400hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387802
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998734
SamplesBILGI_BIOE
Known GenesHNF1B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953888
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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