A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132637



Internal ID19281926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:45804601..45811701hg38UCSC Ensembl
Outerchr7:45844200..45851300hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg387101
hg197101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987424
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132637
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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