A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974200



Internal ID18890249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:2834439..2834538hg38UCSC Ensembl
Outerchr6:2834673..2834772hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124018
Supporting Variants
SamplesKWS2
Known GenesSERPINB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974200
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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