A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964190



Internal ID19239759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24192610..24197810hg38UCSC Ensembl
Outerchr1:24519100..24524300hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120976
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964190
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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