A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145131



Internal ID18927102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:45920601..45921301hg38UCSC Ensembl
Outerchr7:45960200..45960900hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982213
SamplesKWS1
Known GenesIGFBP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145131
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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