A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263117



Internal ID20830157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1351233..2522922hg38UCSC Ensembl
chr4:1345021..2524649hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381171690
hg191179629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567523
Supporting Variants
Samples
Known GenesC4orf48, CRIPAK, FAM53A, FGFR3, HAUS3, LETM1, LOC402160, MIR4800, MIR943, MXD4, NAT8L, NELFA, POLN, RNF4, SCARNA22, SLBP, TACC3, TMEM129, UVSSA, WHSC1, ZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263117
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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