A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109823



Internal ID18923071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:150078339..150078402hg38UCSC Ensembl
Outerchr6:150399475..150399538hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958203
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109823
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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