A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999971



Internal ID17292923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37378798..37406597hg38UCSC Ensembl
Outerchr20:36007201..36035000hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3827800
hg1927800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954032
Supporting Variants
SamplesBILGI_BIOE
Known GenesSRC
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999971
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