A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612708



Internal ID20985779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122094701..122162900hg38UCSC Ensembl
chr7:121734755..121802954hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3868200
hg1968200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151843
Samples
Known GenesAASS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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