A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977740



Internal ID19236786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:257400..382500hg38UCSC Ensembl
Outerchr6:257400..382500hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38125101
hg19125101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124934
Supporting Variants
SamplesKWS2
Known GenesDUSP22
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977740
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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