A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995342



Internal ID19208367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:121521579..121521649hg38UCSC Ensembl
Outerchr10:123281093..123281163hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113340
Supporting Variants
SamplesKWS1
Known GenesFGFR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3995342
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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