A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131597



Internal ID19256222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:157278905..157282201hg38UCSC Ensembl
Outerchr6:157699937..157703233hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3419n106
Supporting Variantsnssv3986050
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131597
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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