A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435353



Internal ID21092906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156015125..156017545hg38UCSC Ensembl
chr7:155807819..155810239hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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