A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119425



Internal ID19259818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:119944345..119945445hg38UCSC Ensembl
Outerchr4:120865500..120866600hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2893n106
Supporting Variantsnssv3959868
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119425
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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