A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997490



Internal ID17290442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:88946582..88948181hg38UCSC Ensembl
Outerchr6:89656301..89657900hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950479
Supporting Variants
SamplesBILGI_BIOE
Known GenesRNGTT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997490
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer