A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435206



Internal ID21092759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138999396..139077532hg38UCSC Ensembl
chr7:138684142..138762278hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3878137
hg1978137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7131n223
Supporting Variantsnssv18234414
Samples
Known GenesZC3HAV1, ZC3HAV1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435206
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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