A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131853



Internal ID19265266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186549226..186549283hg38UCSC Ensembl
Outerchr4:187470380..187470437hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986431
SamplesKWS1
Known GenesMTNR1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131853
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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