A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958446



Internal ID17307319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:75663968..75664062hg38UCSC Ensembl
Outerchr7:75293286..75293380hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004802
SamplesBILGI_BIOE
Known GenesHIP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958446
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