A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421445



Internal ID21078998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149608748..149649189hg38UCSC Ensembl
chr7:149305839..149346280hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3840442
hg1940442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154044
Samples
Known GenesZNF767
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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