A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613019



Internal ID20986090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41719014..41719777hg38UCSC Ensembl
chr7:41758612..41759375hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154454
Samples
Known GenesINHBA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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