A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996971



Internal ID17289923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:124466322..124513521hg38UCSC Ensembl
Outerchr9:127228601..127275800hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3847200
hg1947200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950942
Supporting Variants
SamplesBILGI_BIOE
Known GenesNR5A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996971
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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