A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619912



Internal ID20992983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74216862..74274096hg38UCSC Ensembl
chr7:73631192..73688426hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3857235
hg1957235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232435
Samples
Known GenesLAT2, RFC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619912
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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