A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984395



Internal ID18867221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1355020..1356820hg38UCSC Ensembl
Outerchr1:1290400..1292200hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136054
Supporting Variants
SamplesKWS1
Known GenesMXRA8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984395
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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