A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603906



Internal ID20976977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64087756..64357825hg38UCSC Ensembl
chr7:63548134..63818203hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38270070
hg19270070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224211
Samples
Known GenesZNF679, ZNF735, ZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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