A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112485



Internal ID18903265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:108900845..108900956hg38UCSC Ensembl
Outerchr9:111663125..111663236hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3966575
SamplesKWS2
Known GenesIKBKAP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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