A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608526



Internal ID20981597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21486731..21487370hg38UCSC Ensembl
chr7:21526349..21526988hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156968
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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