A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604176



Internal ID20977247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10671423..11457217hg38UCSC Ensembl
chr7:10711050..11496844hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38785795
hg19785795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235330
Samples
Known GenesNDUFA4, PHF14, THSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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