A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951201



Internal ID16953388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135647755..135770054hg38UCSC Ensembl
Outerchr9:138539601..138661900hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38122300
hg19122300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997037
SamplesBILGI_BIOE
Known GenesKCNT1, LCN9, SOHLH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951201
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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