A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604857



Internal ID20977928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87816848..87817538hg38UCSC Ensembl
chr7:87446163..87446853hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161875
Samples
Known GenesRUNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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