A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998515



Internal ID16944781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71677016..71686615hg38UCSC Ensembl
Outerchr7:71142001..71151600hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950542
Supporting Variants
SamplesBILGI_BIOE
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998515
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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