A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975011



Internal ID18891550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:44207991..44208058hg38UCSC Ensembl
Outerchr6:44175728..44175795hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137077
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975011
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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