A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145121



Internal ID18932493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1236164..1236864hg38UCSC Ensembl
Outerchr7:1275800..1276500hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982203
SamplesKWS1
Known GenesUNCX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145121
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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