A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157586



Internal ID20724626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50769585..50770106hg38UCSC Ensembl
chr7:50837282..50837803hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600138
Supporting Variants
Samples
Known GenesGRB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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