A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000961



Internal ID17293913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:84080553..84080884hg38UCSC Ensembl
Outerchr7:83709869..83710200hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957578
Supporting Variants
SamplesBILGI_BIOE
Known GenesSEMA3A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000961
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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