A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605681



Internal ID20978752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116395221..116397092hg38UCSC Ensembl
chr7:116035275..116037146hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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