A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276035



Internal ID20843075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45642996..53582758hg38UCSC Ensembl
chr7:45682595..53650451hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg387939763
hg197967857
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572893
Supporting Variants
Samples
Known GenesABCA13, ADCY1, C7orf57, C7orf65, C7orf69, C7orf72, CDC14C, COBL, DDC, FIGNL1, GRB10, HUS1, IGFBP1, IGFBP3, IKZF1, LINC00525, LOC100129427, LOC101929086, PKD1L1, POM121L12, SEPT7P2, SUN3, TNS3, UPP1, VWC2, ZPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276035
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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