A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605465



Internal ID20978536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30954756..30955501hg38UCSC Ensembl
chr7:30994371..30995116hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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