A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980958



Internal ID19224857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73529796..73558496hg38UCSC Ensembl
Outerchr14:73996500..74025200hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828701
hg1928701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118282
Supporting Variants
SamplesKWS1
Known GenesACOT1, HEATR4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980958
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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