A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113625



Internal ID19260219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:23925343..23925396hg38UCSC Ensembl
Outerchr14:24394552..24394605hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983807, nssv3990831
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113625
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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