A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563914



Internal ID20936985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47665812..51312144hg38UCSC Ensembl
chr7:47705410..51379841hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg383646333
hg193674432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274518
Samples
Known GenesABCA13, C7orf57, C7orf69, C7orf72, CDC14C, COBL, DDC, FIGNL1, GRB10, HUS1, IKZF1, LINC00525, LOC100129427, PKD1L1, SUN3, UPP1, VWC2, ZPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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