A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610955



Internal ID20984026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54575477..54576087hg38UCSC Ensembl
chr7:54643170..54643780hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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