A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949967



Internal ID16952154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143382508..143399907hg38UCSC Ensembl
Outerchr7:143079601..143097000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3817400
hg1917400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998608
SamplesBILGI_BIOE
Known GenesEPHA1, MIR6892, ZYX
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949967
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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