A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607216



Internal ID20980287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43932601..43934800hg38UCSC Ensembl
chr7:43972200..43974399hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154584
Samples
Known GenesUBE2D4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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