A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003571



Internal ID16949837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:162011357..162011533hg38UCSC Ensembl
Outerchr6:162432389..162432565hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958348
Supporting Variants
SamplesBILGI_BIOE
Known GenesPARK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003571
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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