A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951697



Internal ID17300571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33371103..33374602hg38UCSC Ensembl
Outerchr9:33371101..33374600hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999386
SamplesBILGI_BIOE
Known GenesNFX1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951697
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