A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004934



Internal ID16951200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:67927357..67927427hg38UCSC Ensembl
Outerchr10:69687114..69687184hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958575
Supporting Variants
SamplesBILGI_BIOE
Known GenesHERC4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004934
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