A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605761



Internal ID20978832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40354032..40446033hg38UCSC Ensembl
chr7:40393631..40485632hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3892002
hg1992002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6658n223
Supporting Variantsnssv18237066
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605761
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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