A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612607



Internal ID20985678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74257325..74258928hg38UCSC Ensembl
chr7:73671655..73673258hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381604
hg191604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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