A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956956



Internal ID17305829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:2972014..2972207hg38UCSC Ensembl
Outerchr6:2972248..2972441hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003623
SamplesBILGI_BIOE
Known GenesSERPINB6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956956
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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