A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607464



Internal ID20980535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124568073..124568600hg38UCSC Ensembl
chr7:124208127..124208654hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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