A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619762



Internal ID20992833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12500291..12672668hg38UCSC Ensembl
chr7:12539917..12712293hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38172378
hg19172377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6580n223
Supporting Variantsnssv18150242
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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