A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610224



Internal ID20983295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75719381..75797393hg38UCSC Ensembl
chr7:75348699..75426711hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3878013
hg1978013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6911n223
Supporting Variantsnssv18217727
Samples
Known GenesCCL26, HIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610224
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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