A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001778



Internal ID17294730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:11099444..11101843hg38UCSC Ensembl
Outerchr1:11159501..11161900hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955233
Supporting Variants
SamplesBILGI_BIOE
Known GenesEXOSC10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001778
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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