A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610977



Internal ID20984048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17979373..17980522hg38UCSC Ensembl
chr7:18018996..18020145hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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