A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950701



Internal ID16952888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:43418430..43453929hg38UCSC Ensembl
Outerchr1:43884101..43919600hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3835500
hg1935500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997138
SamplesBILGI_BIOE
Known GenesHYI, MIR6735, SZT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950701
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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