A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131791



Internal ID19266753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:41337391..41337474hg38UCSC Ensembl
Outerchr4:41339408..41339491hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986337
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131791
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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