A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950821



Internal ID16953008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:30896486..30924685hg38UCSC Ensembl
Outerchr7:30936101..30964300hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3828200
hg1928200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997625
SamplesBILGI_BIOE
Known GenesAQP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950821
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