A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968396



Internal ID18899177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:7782940..7784440hg38UCSC Ensembl
Outerchr1:7843000..7844500hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121747
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968396
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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