A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608284



Internal ID20981355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36077230..36241595hg38UCSC Ensembl
chr7:36116840..36281204hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38164366
hg19164365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153723
Samples
Known GenesEEPD1, LOC101928618
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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