A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130806



Internal ID18927272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:43998006..43998059hg38UCSC Ensembl
Outerchr19:44502158..44502211hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967504
SamplesKWS1
Known GenesZNF155
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130806
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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