A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617698



Internal ID20990769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75695611..75696023hg38UCSC Ensembl
chr7:75324929..75325341hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226526
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617698
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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