A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126776



Internal ID19262141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:25948980..25952480hg38UCSC Ensembl
Outerchr7:25988600..25992100hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985048
SamplesKWS1
Known GenesMIR148A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126776
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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