A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950785



Internal ID16952972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1195865..1371564hg38UCSC Ensembl
Outerchr7:1235501..1411200hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38175700
hg19175700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997589
SamplesBILGI_BIOE
Known GenesUNCX
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950785
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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