A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600936



Internal ID20974007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57137444..57138386hg38UCSC Ensembl
chr7:57205151..57206093hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157222
Samples
Known GenesZNF479
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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