A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981709



Internal ID19207185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:3157366..3158366hg38UCSC Ensembl
Outerchr6:3157600..3158600hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145089
Supporting Variants
SamplesKWS1
Known GenesTUBB2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981709
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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