A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949965



Internal ID16952152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:142862343..142878755hg38UCSC Ensembl
Outerchr7:142560101..142576500hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3816413
hg1916400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998606
SamplesBILGI_BIOE
Known GenesEPHB6, TRPV6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949965
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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