A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971297



Internal ID19206516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:121361094..121368894hg38UCSC Ensembl
Outerchr4:122282249..122290049hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg387801
hg197801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122709
Supporting Variants
SamplesKWS1
Known GenesQRFPR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971297
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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