A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605987



Internal ID20979058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112391301..112392300hg38UCSC Ensembl
chr7:112031356..112032355hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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