A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615128



Internal ID20988199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53571916..53606447hg38UCSC Ensembl
chr7:53639609..53674140hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3834532
hg1934532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158457
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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