A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607159



Internal ID20980230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72525732..72847626hg38UCSC Ensembl
chr7:71990717..72318207hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38321895
hg19327491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6906n223
Supporting Variantsnssv18218478
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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