A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951777



Internal ID16953964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128708822..128771221hg38UCSC Ensembl
Outerchr9:131471101..131533500hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3862400
hg1962400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996989
SamplesBILGI_BIOE
Known GenesLOC100506100, PKN3, ZDHHC12, ZER1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951777
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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