A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127968



Internal ID19286874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:71501421..71501483hg38UCSC Ensembl
Outerchr3:71550572..71550634hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957370
SamplesKWS1
Known GenesFOXP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127968
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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