A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984503



Internal ID18860945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:119103788..119104588hg38UCSC Ensembl
Outerchr10:120863300..120864100hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126270
Supporting Variants
SamplesKWS1
Known GenesFAM45A, FAM45B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984503
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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