A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613406



Internal ID20986477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43118705..43120080hg38UCSC Ensembl
chr7:43158304..43159679hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154542
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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