A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121957



Internal ID18927434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79521600..79522400hg38UCSC Ensembl
Outerchr18:77281600..77282400hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1658n106
Supporting Variantsnssv3968628
SamplesKWS2
Known GenesNFATC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121957
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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