A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603041



Internal ID20976112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112829200..112829828hg38UCSC Ensembl
chr7:112469255..112469883hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152803
Samples
Known GenesC7orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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