A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950897



Internal ID17299771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93200119..93215918hg38UCSC Ensembl
Outerchr9:95962401..95978200hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3815800
hg1915800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996930
SamplesBILGI_BIOE
Known GenesWNK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950897
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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