A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112075



Internal ID19279014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107053172..107053330hg38UCSC Ensembl
Outerchr4:107974329..107974487hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n106
Supporting Variantsnssv3957528, nssv3989186
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112075
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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