A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980827



Internal ID18866339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15370601..15371501hg38UCSC Ensembl
Outerchr10:15412600..15413500hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118161
Supporting Variants
SamplesKWS1
Known GenesFAM171A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980827
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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