A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951203



Internal ID16953390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136562849..136770848hg38UCSC Ensembl
Outerchr9:139457301..139665300hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38208000
hg19208000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997039
SamplesBILGI_BIOE
Known GenesAGPAT2, EGFL7, FAM69B, LCN10, LCN15, LCN6, LCN8, LOC100128593, MIR126, MIR6722, SNHG7, SNORA17, SNORA43
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951203
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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