A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217924



Internal ID20784964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:602600..905284hg38UCSC Ensembl
chr7:642237..944921hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38302685
hg19302685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606009
Supporting Variants
Samples
Known GenesADAP1, GET4, HEATR2, PRKAR1B, SUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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