A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111650



Internal ID19266900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107053163..107053329hg38UCSC Ensembl
Outerchr4:107974320..107974486hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n106
Supporting Variantsnssv3964546
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111650
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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