A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985019



Internal ID19211380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:34237323..34237623hg38UCSC Ensembl
Outerchr6:34205100..34205400hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137544
Supporting Variants
SamplesKWS1
Known GenesHMGA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985019
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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