A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615998



Internal ID20989069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16527901..16536700hg38UCSC Ensembl
chr7:16567526..16576325hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152305
Samples
Known GenesLRRC72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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