A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601140



Internal ID20974211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54838064..54999813hg38UCSC Ensembl
chr7:54905757..55067506hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38161750
hg19161750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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