A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619987



Internal ID20993058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44804759..44811322hg38UCSC Ensembl
chr7:44844358..44850921hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg386564
hg196564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6661n223
Supporting Variantsnssv18154621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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