A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600556



Internal ID20973627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73912836..73929870hg38UCSC Ensembl
chr7:73327166..73344200hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3817035
hg1917035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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