A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131961



Internal ID19281535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:49950193..49950249hg38UCSC Ensembl
Outerchr6:49917906..49917962hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986584
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131961
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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