A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113759



Internal ID18914576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15742620..15742681hg38UCSC Ensembl
Outerchr16:15836477..15836538hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969827
SamplesKWS2
Known GenesMYH11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113759
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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