A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977537



Internal ID19239380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160612568..160620268hg38UCSC Ensembl
Outerchr6:161033600..161041300hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg387701
hg197701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115730
Supporting Variants
SamplesKWS2
Known GenesLPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977537
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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