A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969512



Internal ID19229197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1011412..1012312hg38UCSC Ensembl
Outerchr4:1005200..1006100hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122076
Supporting Variants
SamplesKWS2
Known GenesFGFRL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969512
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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